Canonical Allele Identifier: CA1479859431

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124410T= , CM000666.2:g.99124410T=	GRCh38
NC_000004.11:g.100045561T= , CM000666.1:g.100045561T=	GRCh37
NC_000004.10:g.100264584T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.*32A= MANE Select	ENSP00000265512.7:n.*32A=
ENST00000265512.11:c.*32A=	ENSP00000265512.7:n.*32A=
ENST00000505590.5:c.*32A=	ENSP00000425416.1:n.*32A=
ENST00000508393.5:c.*32A=	ENSP00000424630.1:n.*32A=
ENST00000509471.5:c.529A=	ENSP00000424583.1:n.529A=
ENST00000629236.2:c.1172A=	ENSP00000486450.1:p.Asp391=
NM_000670.3:c.*32A=	NP_000661.2:n.*32A=
NM_000670.4:c.*32A=	NP_000661.2:n.*32A=
NM_001306171.1:c.*32A=	NP_001293100.1:n.*32A=
NM_001306172.1:c.*32A=	NP_001293101.1:n.*32A=
NR_037884.1:n.429-9145T=
XR_938685.1:n.1514A=
XR_938686.1:n.1505A=
XR_938687.1:n.1378A=
NM_000670.5:c.*32A= MANE Select	NP_000661.2:n.*32A=
NM_001306171.2:c.*32A=	NP_001293100.1:n.*32A=
NM_001306172.2:c.*32A=	NP_001293101.1:n.*32A=