Canonical Allele Identifier: CA1479860713

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127301G= , CM000666.2:g.99127301G=	GRCh38
NC_000004.11:g.100048452G= , CM000666.1:g.100048452G=	GRCh37
NC_000004.10:g.100267475G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.887C= MANE Select	ENSP00000265512.7:p.Thr296=
ENST00000265512.11:c.887C=	ENSP00000265512.7:p.Thr296=
ENST00000505590.5:c.944C=	ENSP00000425416.1:p.Thr315=
ENST00000506705.5:c.*861C=	ENSP00000426667.1:n.*861C=
ENST00000508393.5:c.944C=	ENSP00000424630.1:p.Thr315=
ENST00000509471.5:c.334-569C=	ENSP00000424583.1:n.334-569C=
ENST00000629236.2:c.887C=	ENSP00000486450.1:p.Thr296=
NM_000670.3:c.887C=	NP_000661.2:p.Thr296=
NM_000670.4:c.887C=	NP_000661.2:p.Thr296=
NM_001306171.1:c.944C=	NP_001293100.1:p.Thr315=
NM_001306172.1:c.944C=	NP_001293101.1:p.Thr315=
NR_037884.1:n.429-6254G=
XR_938685.1:n.1115C=
XR_938686.1:n.1106C=
XR_938687.1:n.979C=
NM_000670.5:c.887C= MANE Select	NP_000661.2:p.Thr296=
NM_001306171.2:c.944C=	NP_001293100.1:p.Thr315=
NM_001306172.2:c.944C=	NP_001293101.1:p.Thr315=