Canonical Allele Identifier: CA1996392118

Gene: DYNC2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103125139T= , CM000673.2:g.103125139T=	GRCh38
NC_000011.9:g.102995868T= , CM000673.1:g.102995868T=	GRCh37
NC_000011.8:g.102501078T=	NCBI36
NG_016423.1:g.20709T=
NG_016423.2:g.20709T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.1701T= MANE Plus Clinical	ENSP00000497174.1:p.Asn567=
ENST00000375735.7:c.1701T= MANE Select	ENSP00000364887.2:p.Asn567=
ENST00000648198.1:c.1701T=	ENSP00000497329.1:p.Asn567=
ENST00000649323.1:c.1701T=	ENSP00000497581.1:p.Asn567=
ENST00000650373.1:c.1701T=	ENSP00000497174.1:p.Asn567=
ENST00000334267.11:c.1701T=	ENSP00000334021.7:p.Asn567=
ENST00000375735.6:c.1701T=	ENSP00000364887.2:p.Asn567=
ENST00000398093.7:c.1701T=	ENSP00000381167.3:p.Asn567=
NM_001080463.1:c.1701T=	NP_001073932.1:p.Asn567=
NM_001377.2:c.1701T=	NP_001368.2:p.Asn567=
XM_006718903.2:c.1701T=	XP_006718966.1:p.Asn567=
XM_017018291.1:c.1701T=	XP_016873780.1:p.Asn567=
XM_017018292.1:c.1083T=	XP_016873781.1:p.Asn361=
XM_017018293.1:c.1701T=	XP_016873782.1:p.Asn567=
NM_001377.3:c.1701T= MANE Select	NP_001368.2:p.Asn567=
NM_001080463.2:c.1701T= MANE Plus Clinical	NP_001073932.1:p.Asn567=