Canonical Allele Identifier: CA1996413803

Gene: DYNC2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103173266T= , CM000673.2:g.103173266T=	GRCh38
NC_000011.9:g.103043995T= , CM000673.1:g.103043995T=	GRCh37
NC_000011.8:g.102549205T=	NCBI36
NG_016423.1:g.68836T=
NG_016423.2:g.68836T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.5519T= MANE Plus Clinical	ENSP00000497174.1:p.Val1840=
ENST00000375735.7:c.5519T= MANE Select	ENSP00000364887.2:p.Val1840=
ENST00000649323.1:c.*3064T=	ENSP00000497581.1:n.*3064T=
ENST00000650373.1:c.5519T=	ENSP00000497174.1:p.Val1840=
ENST00000334267.11:c.2205+38847T=	ENSP00000334021.7:n.2205+38847T=
ENST00000375735.6:c.5519T=	ENSP00000364887.2:p.Val1840=
ENST00000398093.7:c.5519T=	ENSP00000381167.3:p.Val1840=
NM_001080463.1:c.5519T=	NP_001073932.1:p.Val1840=
NM_001377.2:c.5519T=	NP_001368.2:p.Val1840=
XM_006718903.2:c.5519T=	XP_006718966.1:p.Val1840=
XM_017018291.1:c.5519T=	XP_016873780.1:p.Val1840=
XM_017018292.1:c.4901T=	XP_016873781.1:p.Val1634=
XM_017018293.1:c.5519T=	XP_016873782.1:p.Val1840=
NM_001377.3:c.5519T= MANE Select	NP_001368.2:p.Val1840=
NM_001080463.2:c.5519T= MANE Plus Clinical	NP_001073932.1:p.Val1840=