Canonical Allele Identifier: CA476607058

Gene: DYNC2H1

Linked Data

• MyVariant Identifiers: chr11:g.103044017T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103173288T>A , CM000673.2:g.103173288T>A	GRCh38
NC_000011.9:g.103044017T>A , CM000673.1:g.103044017T>A	GRCh37
NC_000011.8:g.102549227T>A	NCBI36
NG_016423.1:g.68858T>A
NG_016423.2:g.68858T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.5541T>A MANE Plus Clinical	ENSP00000497174.1:p.Ala1847=
ENST00000375735.7:c.5541T>A MANE Select	ENSP00000364887.2:p.Ala1847=
ENST00000649323.1:c.*3086T>A	ENSP00000497581.1:n.*3086T>A
ENST00000650373.1:c.5541T>A	ENSP00000497174.1:p.Ala1847=
ENST00000334267.11:c.2205+38869T>A	ENSP00000334021.7:n.2205+38869T>A
ENST00000375735.6:c.5541T>A	ENSP00000364887.2:p.Ala1847=
ENST00000398093.7:c.5541T>A	ENSP00000381167.3:p.Ala1847=
NM_001080463.1:c.5541T>A	NP_001073932.1:p.Ala1847=
NM_001377.2:c.5541T>A	NP_001368.2:p.Ala1847=
XM_006718903.2:c.5541T>A	XP_006718966.1:p.Ala1847=
XM_017018291.1:c.5541T>A	XP_016873780.1:p.Ala1847=
XM_017018292.1:c.4923T>A	XP_016873781.1:p.Ala1641=
XM_017018293.1:c.5541T>A	XP_016873782.1:p.Ala1847=
NM_001377.3:c.5541T>A MANE Select	NP_001368.2:p.Ala1847=
NM_001080463.2:c.5541T>A MANE Plus Clinical	NP_001073932.1:p.Ala1847=