Canonical Allele Identifier: CA1479867805

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99144276A= , CM000666.2:g.99144276A=	GRCh38
NC_000004.11:g.100065427A= , CM000666.1:g.100065427A=	GRCh37
NC_000004.10:g.100284450A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.-54T= MANE Select	ENSP00000265512.7:n.-54T=
ENST00000265512.11:c.-54T=	ENSP00000265512.7:n.-54T=
ENST00000504581.1:n.170-1496T=
ENST00000504894.1:c.-115T=	ENSP00000427261.1:n.-115T=
ENST00000505590.5:c.-137T=	ENSP00000425416.1:n.-137T=
ENST00000506705.5:c.-137T=	ENSP00000426667.1:n.-137T=
ENST00000508393.5:c.-145T=	ENSP00000424630.1:n.-145T=
ENST00000629236.2:c.-54T=	ENSP00000486450.1:n.-54T=
NM_000670.3:c.-54T=	NP_000661.2:n.-54T=
NM_000670.4:c.-54T=	NP_000661.2:n.-54T=
NM_001306171.1:c.-145T=	NP_001293100.1:n.-145T=
NM_001306172.1:c.-137T=	NP_001293101.1:n.-137T=
NR_037884.1:n.680-10269A=
XR_938685.1:n.35T=
XR_938686.1:n.18T=
XR_938687.1:n.39T=
NM_000670.5:c.-54T= MANE Select	NP_000661.2:n.-54T=
NM_001306171.2:c.-145T=	NP_001293100.1:n.-145T=
NM_001306172.2:c.-137T=	NP_001293101.1:n.-137T=