Canonical Allele Identifier: CA2662657535

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201625950-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201625950_201625951insAG , CM000664.2:g.201625950_201625951insAG	GRCh38
NC_000002.11:g.202490673_202490674insAG , CM000664.1:g.202490673_202490674insAG	GRCh37
NC_000002.10:g.202198918_202198919insAG	NCBI36
NG_032049.1:g.22579_22580insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.955+75_955+76insCT
ENST00000621467.5:c.1033+75_1033+76insCT	ENSP00000480508.2:n.1033+75_1033+76insCT
ENST00000686475.1:n.1099+75_1099+76insCT
ENST00000409883.7:c.1159+75_1159+76insCT MANE Select	ENSP00000386264.2:n.1159+75_1159+76insCT
ENST00000286196.9:c.*723+75_*723+76insCT	ENSP00000286196.5:n.*723+75_*723+76insCT
ENST00000409444.6:c.1135+75_1135+76insCT	ENSP00000387203.2:n.1135+75_1135+76insCT
ENST00000409883.6:c.1159+75_1159+76insCT	ENSP00000386264.2:n.1159+75_1159+76insCT
ENST00000471318.5:n.387+75_387+76insCT
ENST00000495329.1:n.298+75_298+76insCT
ENST00000621467.4:c.1135+75_1135+76insCT	ENSP00000480508.1:n.1135+75_1135+76insCT
NM_001044385.2:c.1159+75_1159+76insCT	NP_001037850.1:n.1159+75_1159+76insCT
NM_152388.3:c.1135+75_1135+76insCT	NP_689601.2:n.1135+75_1135+76insCT
NM_001044385.3:c.1159+75_1159+76insCT MANE Select	NP_001037850.1:n.1159+75_1159+76insCT
NM_152388.4:c.1135+75_1135+76insCT	NP_689601.2:n.1135+75_1135+76insCT