Canonical Allele Identifier: CA1479863703

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99134466C= , CM000666.2:g.99134466C=	GRCh38
NC_000004.11:g.100055617C= , CM000666.1:g.100055617C=	GRCh37
NC_000004.10:g.100274640C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265512.12:c.582+2000G= MANE Select	ENSP00000265512.7:n.582+2000G=
ENST00000265512.11:c.582+2000G=	ENSP00000265512.7:n.582+2000G=
ENST00000503416.5:n.595+2000G=
ENST00000504125.1:c.528+2000G=	ENSP00000427525.1:n.528+2000G=
ENST00000505590.5:c.639+2000G=	ENSP00000425416.1:n.639+2000G=
ENST00000506705.5:c.*556+2000G=	ENSP00000426667.1:n.*556+2000G=
ENST00000508393.5:c.639+2000G=	ENSP00000424630.1:n.639+2000G=
ENST00000509471.5:c.72+2000G=	ENSP00000424583.1:n.72+2000G=
ENST00000512499.5:c.639+2000G=	ENSP00000423571.1:n.639+2000G=
ENST00000629236.2:c.582+2000G=	ENSP00000486450.1:n.582+2000G=
NM_000670.3:c.582+2000G=	NP_000661.2:n.582+2000G=
NM_000670.4:c.582+2000G=	NP_000661.2:n.582+2000G=
NM_001306171.1:c.639+2000G=	NP_001293100.1:n.639+2000G=
NM_001306172.1:c.639+2000G=	NP_001293101.1:n.639+2000G=
NR_037884.1:n.679+661C=
XR_938685.1:n.810+2000G=
XR_938686.1:n.801+2000G=
XR_938687.1:n.674+2000G=
NM_000670.5:c.582+2000G= MANE Select	NP_000661.2:n.582+2000G=
NM_001306171.2:c.639+2000G=	NP_001293100.1:n.639+2000G=
NM_001306172.2:c.639+2000G=	NP_001293101.1:n.639+2000G=