Canonical Allele Identifier: CA1479860286

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99126335A= , CM000666.2:g.99126335A=	GRCh38
NC_000004.11:g.100047486A= , CM000666.1:g.100047486A=	GRCh37
NC_000004.10:g.100266509A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1118+259T= MANE Select	ENSP00000265512.7:n.1118+259T=
ENST00000265512.11:c.1118+259T=	ENSP00000265512.7:n.1118+259T=
ENST00000505590.5:c.1175+259T=	ENSP00000425416.1:n.1175+259T=
ENST00000508393.5:c.1175+259T=	ENSP00000424630.1:n.1175+259T=
ENST00000509471.5:c.472+259T=	ENSP00000424583.1:n.472+259T=
ENST00000629236.2:c.1118+259T=	ENSP00000486450.1:n.1118+259T=
NM_000670.3:c.1118+259T=	NP_000661.2:n.1118+259T=
NM_000670.4:c.1118+259T=	NP_000661.2:n.1118+259T=
NM_001306171.1:c.1175+259T=	NP_001293100.1:n.1175+259T=
NM_001306172.1:c.1175+259T=	NP_001293101.1:n.1175+259T=
NR_037884.1:n.429-7220A=
XR_938685.1:n.1346+259T=
XR_938686.1:n.1337+259T=
XR_938687.1:n.1210+259T=
NM_000670.5:c.1118+259T= MANE Select	NP_000661.2:n.1118+259T=
NM_001306171.2:c.1175+259T=	NP_001293100.1:n.1175+259T=
NM_001306172.2:c.1175+259T=	NP_001293101.1:n.1175+259T=