Canonical Allele Identifier: CA1996410752

Gene: DYNC2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103165935A= , CM000673.2:g.103165935A=	GRCh38
NC_000011.9:g.103036664A= , CM000673.1:g.103036664A=	GRCh37
NC_000011.8:g.102541874A=	NCBI36
NG_016423.1:g.61505A=
NG_016423.2:g.61505A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.4649A= MANE Plus Clinical	ENSP00000497174.1:p.Asp1550=
ENST00000375735.7:c.4649A= MANE Select	ENSP00000364887.2:p.Asp1550=
ENST00000649323.1:c.*2194A=	ENSP00000497581.1:n.*2194A=
ENST00000650373.1:c.4649A=	ENSP00000497174.1:p.Asp1550=
ENST00000334267.11:c.2205+31516A=	ENSP00000334021.7:n.2205+31516A=
ENST00000375735.6:c.4649A=	ENSP00000364887.2:p.Asp1550=
ENST00000398093.7:c.4649A=	ENSP00000381167.3:p.Asp1550=
NM_001080463.1:c.4649A=	NP_001073932.1:p.Asp1550=
NM_001377.2:c.4649A=	NP_001368.2:p.Asp1550=
XM_006718903.2:c.4649A=	XP_006718966.1:p.Asp1550=
XM_017018291.1:c.4649A=	XP_016873780.1:p.Asp1550=
XM_017018292.1:c.4031A=	XP_016873781.1:p.Asp1344=
XM_017018293.1:c.4649A=	XP_016873782.1:p.Asp1550=
NM_001377.3:c.4649A= MANE Select	NP_001368.2:p.Asp1550=
NM_001080463.2:c.4649A= MANE Plus Clinical	NP_001073932.1:p.Asp1550=