Canonical Allele Identifier: CA3020481

Gene: ADH1C ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99347033C= , CM000666.2:g.99347033C=	GRCh38
NG_011718.1:g.10728G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515683.6:c.232G= (ADH1C) MANE Select	ENSP00000426083.1:p.Gly78=
ENST00000639454.1:c.18+5625G= (ADH1B)	ENSP00000491622.1:n.18+5625G=
ENST00000505942.2:n.301G= (ADH1C)
ENST00000510055.5:c.112G= (ADH1C)	ENSP00000478439.1:p.Gly38=
ENST00000511397.3:c.130G= (ADH1C)	ENSP00000478545.1:p.Gly44=
ENST00000515683.5:c.232G= (ADH1C)	ENSP00000426083.1:p.Gly78=
NM_000669.4:c.232G= (ADH1C)	NP_000660.1:p.Gly78=
NR_133005.1:n.602G= (ADH1C)
XM_011531588.1:c.130G= (ADH1C)	XP_011529890.1:p.Gly44=
XM_011531589.1:c.112G= (ADH1C)	XP_011529891.1:p.Gly38=
NM_000669.5:c.232G= (ADH1C) MANE Select	NP_000660.1:p.Gly78=
NR_133005.2:n.303G= (ADH1C)