Canonical Allele Identifier: CA1479867802

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99144263A= , CM000666.2:g.99144263A=	GRCh38
NC_000004.11:g.100065414A= , CM000666.1:g.100065414A=	GRCh37
NC_000004.10:g.100284437A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.-41T= MANE Select	ENSP00000265512.7:n.-41T=
ENST00000265512.11:c.-41T=	ENSP00000265512.7:n.-41T=
ENST00000504125.1:c.-41T=	ENSP00000427525.1:n.-41T=
ENST00000504581.1:n.170-1483T=
ENST00000504894.1:c.-102T=	ENSP00000427261.1:n.-102T=
ENST00000505590.5:c.-124T=	ENSP00000425416.1:n.-124T=
ENST00000506705.5:c.-124T=	ENSP00000426667.1:n.-124T=
ENST00000508393.5:c.-132T=	ENSP00000424630.1:n.-132T=
ENST00000629236.2:c.-41T=	ENSP00000486450.1:n.-41T=
NM_000670.3:c.-41T=	NP_000661.2:n.-41T=
NM_000670.4:c.-41T=	NP_000661.2:n.-41T=
NM_001306171.1:c.-132T=	NP_001293100.1:n.-132T=
NM_001306172.1:c.-124T=	NP_001293101.1:n.-124T=
NR_037884.1:n.680-10282A=
XR_938685.1:n.48T=
XR_938686.1:n.31T=
XR_938687.1:n.52T=
NM_000670.5:c.-41T= MANE Select	NP_000661.2:n.-41T=
NM_001306171.2:c.-132T=	NP_001293100.1:n.-132T=
NM_001306172.2:c.-124T=	NP_001293101.1:n.-124T=