Canonical Allele Identifier: CA1479860615

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127088T= , CM000666.2:g.99127088T=	GRCh38
NC_000004.11:g.100048239T= , CM000666.1:g.100048239T=	GRCh37
NC_000004.10:g.100267262T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.979+121A= MANE Select	ENSP00000265512.7:n.979+121A=
ENST00000265512.11:c.979+121A=	ENSP00000265512.7:n.979+121A=
ENST00000505590.5:c.1036+121A=	ENSP00000425416.1:n.1036+121A=
ENST00000506705.5:c.*953+121A=	ENSP00000426667.1:n.*953+121A=
ENST00000508393.5:c.1036+121A=	ENSP00000424630.1:n.1036+121A=
ENST00000509471.5:c.334-356A=	ENSP00000424583.1:n.334-356A=
ENST00000629236.2:c.979+121A=	ENSP00000486450.1:n.979+121A=
NM_000670.3:c.979+121A=	NP_000661.2:n.979+121A=
NM_000670.4:c.979+121A=	NP_000661.2:n.979+121A=
NM_001306171.1:c.1036+121A=	NP_001293100.1:n.1036+121A=
NM_001306172.1:c.1036+121A=	NP_001293101.1:n.1036+121A=
NR_037884.1:n.429-6467T=
XR_938685.1:n.1207+121A=
XR_938686.1:n.1198+121A=
XR_938687.1:n.1071+121A=
NM_000670.5:c.979+121A= MANE Select	NP_000661.2:n.979+121A=
NM_001306171.2:c.1036+121A=	NP_001293100.1:n.1036+121A=
NM_001306172.2:c.1036+121A=	NP_001293101.1:n.1036+121A=