Canonical Allele Identifier: CA2615751338

Gene: DYNC2H1

Linked Data

• gnomAD v4: 11-103256365-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103256365A>C , CM000673.2:g.103256365A>C	GRCh38
NC_000011.9:g.103127094A>C , CM000673.1:g.103127094A>C	GRCh37
NC_000011.8:g.102632304A>C	NCBI36
NG_016423.1:g.151935A>C
NG_016423.2:g.151935A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.10482+125A>C MANE Plus Clinical	ENSP00000497174.1:n.10482+125A>C
ENST00000375735.7:c.10461+125A>C MANE Select	ENSP00000364887.2:n.10461+125A>C
ENST00000650373.1:c.10482+125A>C	ENSP00000497174.1:n.10482+125A>C
ENST00000334267.11:c.2205+121946A>C	ENSP00000334021.7:n.2205+121946A>C
ENST00000375735.6:c.10461+125A>C	ENSP00000364887.2:n.10461+125A>C
ENST00000398093.7:c.10482+125A>C	ENSP00000381167.3:n.10482+125A>C
NM_001080463.1:c.10482+125A>C	NP_001073932.1:n.10482+125A>C
NM_001377.2:c.10461+125A>C	NP_001368.2:n.10461+125A>C
XM_006718903.2:c.10440+125A>C	XP_006718966.1:n.10440+125A>C
XM_017018291.1:c.10461+125A>C	XP_016873780.1:n.10461+125A>C
XM_017018292.1:c.9843+125A>C	XP_016873781.1:n.9843+125A>C
NM_001377.3:c.10461+125A>C MANE Select	NP_001368.2:n.10461+125A>C
NM_001080463.2:c.10482+125A>C MANE Plus Clinical	NP_001073932.1:n.10482+125A>C