Canonical Allele Identifier: CA1996420755

Gene: DYNC2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103189794C= , CM000673.2:g.103189794C=	GRCh38
NC_000011.9:g.103060523C= , CM000673.1:g.103060523C=	GRCh37
NC_000011.8:g.102565733C=	NCBI36
NG_016423.1:g.85364C=
NG_016423.2:g.85364C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.7415C= MANE Plus Clinical	ENSP00000497174.1:p.Ser2472=
ENST00000375735.7:c.7415C= MANE Select	ENSP00000364887.2:p.Ser2472=
ENST00000649323.1:c.*4960C=	ENSP00000497581.1:n.*4960C=
ENST00000650373.1:c.7415C=	ENSP00000497174.1:p.Ser2472=
ENST00000334267.11:c.2205+55375C=	ENSP00000334021.7:n.2205+55375C=
ENST00000375735.6:c.7415C=	ENSP00000364887.2:p.Ser2472=
ENST00000398093.7:c.7415C=	ENSP00000381167.3:p.Ser2472=
NM_001080463.1:c.7415C=	NP_001073932.1:p.Ser2472=
NM_001377.2:c.7415C=	NP_001368.2:p.Ser2472=
XM_006718903.2:c.7415C=	XP_006718966.1:p.Ser2472=
XM_017018291.1:c.7415C=	XP_016873780.1:p.Ser2472=
XM_017018292.1:c.6797C=	XP_016873781.1:p.Ser2266=
XM_017018293.1:c.7415C=	XP_016873782.1:p.Ser2472=
NM_001377.3:c.7415C= MANE Select	NP_001368.2:p.Ser2472=
NM_001080463.2:c.7415C= MANE Plus Clinical	NP_001073932.1:p.Ser2472=