Canonical Allele Identifier: CA6254240

Gene: DYNC2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103191521G>A , CM000673.2:g.103191521G>A	GRCh38
NC_000011.9:g.103062250G>A , CM000673.1:g.103062250G>A	GRCh37
NC_000011.8:g.102567460G>A	NCBI36
NG_016423.1:g.87091G>A
NG_016423.2:g.87091G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001377.3:c.7442G>A MANE Select	NP_001368.2:p.Arg2481Gln
ENST00000375735.7:c.7442G>A MANE Select	ENSP00000364887.2:p.Arg2481Gln
NM_001080463.2:c.7442G>A MANE Plus Clinical	NP_001073932.1:p.Arg2481Gln
ENST00000650373.2:c.7442G>A MANE Plus Clinical	ENSP00000497174.1:p.Arg2481Gln
NM_001080463.1:c.7442G>A	NP_001073932.1:p.Arg2481Gln
NM_001377.2:c.7442G>A	NP_001368.2:p.Arg2481Gln
ENST00000334267.11:c.2205+57102G>A	ENSP00000334021.7:n.2205+57102G>A
ENST00000375735.6:c.7442G>A	ENSP00000364887.2:p.Arg2481Gln
ENST00000398093.7:c.7442G>A	ENSP00000381167.3:p.Arg2481Gln
ENST00000649323.1:c.*4987G>A	ENSP00000497581.1:n.*4987G>A
ENST00000650373.1:c.7442G>A	ENSP00000497174.1:p.Arg2481Gln
XM_006718903.2:c.7442G>A	XP_006718966.1:p.Arg2481Gln
XM_017018291.1:c.7442G>A	XP_016873780.1:p.Arg2481Gln
XM_017018292.1:c.6824G>A	XP_016873781.1:p.Arg2275Gln
XM_017018293.1:c.7438-576G>A	XP_016873782.1:n.7438-576G>A