Canonical Allele Identifier: CA1479859435

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124414A= , CM000666.2:g.99124414A=	GRCh38
NC_000004.11:g.100045565A= , CM000666.1:g.100045565A=	GRCh37
NC_000004.10:g.100264588A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.*28T= MANE Select	ENSP00000265512.7:n.*28T=
ENST00000265512.11:c.*28T=	ENSP00000265512.7:n.*28T=
ENST00000505590.5:c.*28T=	ENSP00000425416.1:n.*28T=
ENST00000508393.5:c.*28T=	ENSP00000424630.1:n.*28T=
ENST00000509471.5:c.525T=	ENSP00000424583.1:n.525T=
ENST00000629236.2:c.1168T=	ENSP00000486450.1:p.Ser390=
NM_000670.3:c.*28T=	NP_000661.2:n.*28T=
NM_000670.4:c.*28T=	NP_000661.2:n.*28T=
NM_001306171.1:c.*28T=	NP_001293100.1:n.*28T=
NM_001306172.1:c.*28T=	NP_001293101.1:n.*28T=
NR_037884.1:n.429-9141A=
XR_938685.1:n.1510T=
XR_938686.1:n.1501T=
XR_938687.1:n.1374T=
NM_000670.5:c.*28T= MANE Select	NP_000661.2:n.*28T=
NM_001306171.2:c.*28T=	NP_001293100.1:n.*28T=
NM_001306172.2:c.*28T=	NP_001293101.1:n.*28T=