Canonical Allele Identifier: CA6254936

Gene: DYNC2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103255460C>G , CM000673.2:g.103255460C>G	GRCh38
NC_000011.9:g.103126189C>G , CM000673.1:g.103126189C>G	GRCh37
NC_000011.8:g.102631399C>G	NCBI36
NG_016423.1:g.151030C>G
NG_016423.2:g.151030C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001377.3:c.10252C>G MANE Select	NP_001368.2:p.Gln3418Glu
ENST00000375735.7:c.10252C>G MANE Select	ENSP00000364887.2:p.Gln3418Glu
NM_001080463.2:c.10273C>G MANE Plus Clinical	NP_001073932.1:p.Gln3425Glu
ENST00000650373.2:c.10273C>G MANE Plus Clinical	ENSP00000497174.1:p.Gln3425Glu
NM_001080463.1:c.10273C>G	NP_001073932.1:p.Gln3425Glu
NM_001377.2:c.10252C>G	NP_001368.2:p.Gln3418Glu
ENST00000334267.11:c.2205+121041C>G	ENSP00000334021.7:n.2205+121041C>G
ENST00000375735.6:c.10252C>G	ENSP00000364887.2:p.Gln3418Glu
ENST00000398093.7:c.10273C>G	ENSP00000381167.3:p.Gln3425Glu
ENST00000650373.1:c.10273C>G	ENSP00000497174.1:p.Gln3425Glu
XM_006718903.2:c.10231C>G	XP_006718966.1:p.Gln3411Glu
XM_017018291.1:c.10252C>G	XP_016873780.1:p.Gln3418Glu
XM_017018292.1:c.9634C>G	XP_016873781.1:p.Gln3212Glu