Canonical Allele Identifier: CA424516968

Gene: MYT1L

Linked Data

• MyVariant Identifiers: chr2:g.1921098T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1917326T>G , CM000664.2:g.1917326T>G	GRCh38
NC_000002.11:g.1921098T>G , CM000664.1:g.1921098T>G	GRCh37
NC_000002.10:g.1900105T>G	NCBI36
NG_051313.1:g.419063A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399161.8:c.1491A>C	ENSP00000382114.3:p.Thr497=
ENST00000470954.3:c.986A>C
ENST00000602387.6:c.992A>C
ENST00000647687.2:c.986A>C
ENST00000648430.2:c.992A>C
ENST00000648665.2:c.1491A>C	ENSP00000497115.1:p.Thr497=
ENST00000648753.2:c.992A>C
ENST00000648931.2:c.986A>C
ENST00000648943.2:c.986A>C
ENST00000649641.2:c.1497A>C	ENSP00000497373.2:p.Thr499=
ENST00000649709.2:c.519A>C	ENSP00000497604.2:p.Thr173=
ENST00000649840.2:c.14A>C
ENST00000650399.2:c.506-25039A>C	ENSP00000497900.2:n.506-25039A>C
ENST00000650485.2:c.1491A>C	ENSP00000497068.1:p.Thr497=
ENST00000399161.7:c.1491A>C	ENSP00000382114.3:p.Thr497=
ENST00000428368.7:c.1497A>C	ENSP00000396103.3:p.Thr499=
ENST00000470954.2:c.240A>C	ENSP00000497244.1:p.Thr80=
ENST00000644820.1:c.1497A>C	ENSP00000496210.1:p.Thr499=
ENST00000647618.1:c.1434A>C	ENSP00000497024.1:p.Thr478=
ENST00000647687.1:c.292A>C
ENST00000647694.1:c.1497A>C	ENSP00000497722.1:p.Thr499=
ENST00000647738.2:c.1497A>C MANE Select	ENSP00000497479.2:p.Thr499=
ENST00000647755.1:c.1491A>C	ENSP00000496922.1:p.Thr497=
ENST00000648316.1:c.1491A>C	ENSP00000497870.1:p.Thr497=
ENST00000648318.1:c.1491A>C	ENSP00000496831.1:p.Thr497=
ENST00000648339.1:c.1497A>C	ENSP00000497493.1:p.Thr499=
ENST00000648430.1:c.992A>C
ENST00000648627.1:c.519A>C	ENSP00000497309.1:p.Thr173=
ENST00000648665.1:c.1491A>C	ENSP00000497115.1:p.Thr497=
ENST00000648753.1:c.712A>C
ENST00000648928.1:c.1491A>C	ENSP00000497017.1:p.Thr497=
ENST00000648931.1:c.292A>C
ENST00000648933.1:c.519A>C	ENSP00000497838.1:p.Thr173=
ENST00000648943.1:c.691A>C
ENST00000649207.1:c.1491A>C	ENSP00000496986.1:p.Thr497=
ENST00000649641.1:c.1497A>C	ENSP00000497373.1:p.Thr499=
ENST00000649663.1:c.1497A>C	ENSP00000497273.1:p.Thr499=
ENST00000649709.1:c.519A>C	ENSP00000497604.1:p.Thr173=
ENST00000649810.1:c.1477+4966A>C	ENSP00000498096.1:n.1477+4966A>C
ENST00000649840.1:c.12A>C	ENSP00000496783.1:p.Thr4=
ENST00000650081.1:c.*934A>C	ENSP00000497922.1:n.*934A>C
ENST00000650399.1:c.410-25039A>C	ENSP00000497900.1:n.410-25039A>C
ENST00000650485.1:c.1491A>C	ENSP00000497068.1:p.Thr497=
ENST00000650560.1:c.1494A>C	ENSP00000497816.1:p.Thr498=
ENST00000399161.6:c.1497A>C	ENSP00000382114.2:p.Thr499=
ENST00000428368.6:c.1491A>C	ENSP00000396103.2:p.Thr497=
ENST00000602387.5:c.459A>C	ENSP00000473409.1:p.Thr153=
NM_001303052.1:c.1497A>C	NP_001289981.1:p.Thr499=
NM_015025.3:c.1491A>C	NP_055840.2:p.Thr497=
XM_011510318.1:c.1497A>C	XP_011508620.1:p.Thr499=
XM_011510319.1:c.1497A>C	XP_011508621.1:p.Thr499=
XM_011510320.1:c.1497A>C	XP_011508622.1:p.Thr499=
XM_011510321.1:c.1497A>C	XP_011508623.1:p.Thr499=
XM_011510322.1:c.1497A>C	XP_011508624.1:p.Thr499=
XM_011510323.1:c.1497A>C	XP_011508625.1:p.Thr499=
XM_011510324.1:c.1497A>C	XP_011508626.1:p.Thr499=
XM_011510325.1:c.1491A>C	XP_011508627.1:p.Thr497=
XM_011510326.1:c.1497A>C	XP_011508628.1:p.Thr499=
XM_011510327.1:c.1497A>C	XP_011508629.1:p.Thr499=
XM_011510328.1:c.1497A>C	XP_011508630.1:p.Thr499=
XM_011510329.1:c.1203A>C	XP_011508631.1:p.Thr401=
XM_011510330.1:c.1497A>C	XP_011508632.1:p.Thr499=
XM_011510331.1:c.1497A>C	XP_011508633.1:p.Thr499=
XM_011510332.1:c.1497A>C	XP_011508634.1:p.Thr499=
NM_001329844.1:c.1497A>C	NP_001316773.1:p.Thr499=
NM_001329845.1:c.1497A>C	NP_001316774.1:p.Thr499=
NM_001329846.1:c.1491A>C	NP_001316775.1:p.Thr497=
NM_001329847.1:c.1491A>C	NP_001316776.1:p.Thr497=
NM_001329848.1:c.1491A>C	NP_001316777.1:p.Thr497=
NM_001329849.1:c.1491A>C	NP_001316778.1:p.Thr497=
NM_001329851.1:c.1497A>C	NP_001316780.1:p.Thr499=
NM_001329852.1:c.1491A>C	NP_001316781.1:p.Thr497=
XM_011510320.3:c.1497A>C	XP_011508622.1:p.Thr499=
XM_011510321.2:c.1497A>C	XP_011508623.1:p.Thr499=
XM_011510322.2:c.1497A>C	XP_011508624.1:p.Thr499=
XM_011510324.2:c.1497A>C	XP_011508626.1:p.Thr499=
XM_011510328.2:c.1497A>C	XP_011508630.1:p.Thr499=
XM_011510331.2:c.1497A>C	XP_011508633.1:p.Thr499=
XM_011510332.2:c.1497A>C	XP_011508634.1:p.Thr499=
XM_017003604.1:c.1497A>C	XP_016859093.1:p.Thr499=
XM_017003605.1:c.1497A>C	XP_016859094.1:p.Thr499=
XM_017003606.1:c.1491A>C	XP_016859095.1:p.Thr497=
XM_017003607.2:c.1491A>C	XP_016859096.1:p.Thr497=
XM_017003608.1:c.1497A>C	XP_016859097.1:p.Thr499=
XM_017003611.1:c.1491A>C	XP_016859100.1:p.Thr497=
XM_017003612.1:c.1491A>C	XP_016859101.1:p.Thr497=
XM_017003615.1:c.1497A>C	XP_016859104.1:p.Thr499=
XM_017003616.1:c.1497A>C	XP_016859105.1:p.Thr499=
XM_017003618.1:c.1491A>C	XP_016859107.1:p.Thr497=
XM_017003620.1:c.1203A>C	XP_016859109.1:p.Thr401=
XM_017003621.1:c.1497A>C	XP_016859110.1:p.Thr499=
XM_017003622.1:c.1497A>C	XP_016859111.1:p.Thr499=
NM_001303052.2:c.1497A>C MANE Select	NP_001289981.1:p.Thr499=
NM_001329844.2:c.1497A>C	NP_001316773.1:p.Thr499=
NM_001329846.2:c.1491A>C	NP_001316775.1:p.Thr497=
NM_001329847.2:c.1491A>C	NP_001316776.1:p.Thr497=
NM_001329849.2:c.1491A>C	NP_001316778.1:p.Thr497=
NM_001329851.2:c.1497A>C	NP_001316780.1:p.Thr499=
NM_001329852.2:c.1491A>C	NP_001316781.1:p.Thr497=
NM_015025.4:c.1491A>C	NP_055840.2:p.Thr497=
NM_001329846.3:c.1491A>C	NP_001316775.1:p.Thr497=
NM_001329849.3:c.1491A>C	NP_001316778.1:p.Thr497=
NM_001329851.3:c.1497A>C	NP_001316780.1:p.Thr499=
NM_001329852.3:c.1491A>C	NP_001316781.1:p.Thr497=