Canonical Allele Identifier: CA1996449632

Gene: DYNC2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103256378G= , CM000673.2:g.103256378G=	GRCh38
NC_000011.9:g.103127107G= , CM000673.1:g.103127107G=	GRCh37
NC_000011.8:g.102632317G=	NCBI36
NG_016423.1:g.151948G=
NG_016423.2:g.151948G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.10482+138G= MANE Plus Clinical	ENSP00000497174.1:n.10482+138G=
ENST00000375735.7:c.10461+138G= MANE Select	ENSP00000364887.2:n.10461+138G=
ENST00000650373.1:c.10482+138G=	ENSP00000497174.1:n.10482+138G=
ENST00000334267.11:c.2205+121959G=	ENSP00000334021.7:n.2205+121959G=
ENST00000375735.6:c.10461+138G=	ENSP00000364887.2:n.10461+138G=
ENST00000398093.7:c.10482+138G=	ENSP00000381167.3:n.10482+138G=
NM_001080463.1:c.10482+138G=	NP_001073932.1:n.10482+138G=
NM_001377.2:c.10461+138G=	NP_001368.2:n.10461+138G=
XM_006718903.2:c.10440+138G=	XP_006718966.1:n.10440+138G=
XM_017018291.1:c.10461+138G=	XP_016873780.1:n.10461+138G=
XM_017018292.1:c.9843+138G=	XP_016873781.1:n.9843+138G=
NM_001377.3:c.10461+138G= MANE Select	NP_001368.2:n.10461+138G=
NM_001080463.2:c.10482+138G= MANE Plus Clinical	NP_001073932.1:n.10482+138G=