Canonical Allele Identifier: CA1479860659

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127193G= , CM000666.2:g.99127193G=	GRCh38
NC_000004.11:g.100048344G= , CM000666.1:g.100048344G=	GRCh37
NC_000004.10:g.100267367G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.979+16C= MANE Select	ENSP00000265512.7:n.979+16C=
ENST00000265512.11:c.979+16C=	ENSP00000265512.7:n.979+16C=
ENST00000505590.5:c.1036+16C=	ENSP00000425416.1:n.1036+16C=
ENST00000506705.5:c.*953+16C=	ENSP00000426667.1:n.*953+16C=
ENST00000508393.5:c.1036+16C=	ENSP00000424630.1:n.1036+16C=
ENST00000509471.5:c.334-461C=	ENSP00000424583.1:n.334-461C=
ENST00000629236.2:c.979+16C=	ENSP00000486450.1:n.979+16C=
NM_000670.3:c.979+16C=	NP_000661.2:n.979+16C=
NM_000670.4:c.979+16C=	NP_000661.2:n.979+16C=
NM_001306171.1:c.1036+16C=	NP_001293100.1:n.1036+16C=
NM_001306172.1:c.1036+16C=	NP_001293101.1:n.1036+16C=
NR_037884.1:n.429-6362G=
XR_938685.1:n.1207+16C=
XR_938686.1:n.1198+16C=
XR_938687.1:n.1071+16C=
NM_000670.5:c.979+16C= MANE Select	NP_000661.2:n.979+16C=
NM_001306171.2:c.1036+16C=	NP_001293100.1:n.1036+16C=
NM_001306172.2:c.1036+16C=	NP_001293101.1:n.1036+16C=