Canonical Allele Identifier: CA440304865

Gene: ADH4

Linked Data

• MyVariant Identifiers: chr4:g.100048412A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127261A>T , CM000666.2:g.99127261A>T	GRCh38
NC_000004.11:g.100048412A>T , CM000666.1:g.100048412A>T	GRCh37
NC_000004.10:g.100267435A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.927T>A MANE Select	ENSP00000265512.7:p.Ile309=
ENST00000265512.11:c.927T>A	ENSP00000265512.7:p.Ile309=
ENST00000505590.5:c.984T>A	ENSP00000425416.1:p.Ile328=
ENST00000506705.5:c.*901T>A	ENSP00000426667.1:n.*901T>A
ENST00000508393.5:c.984T>A	ENSP00000424630.1:p.Ile328=
ENST00000509471.5:c.334-529T>A	ENSP00000424583.1:n.334-529T>A
ENST00000629236.2:c.927T>A	ENSP00000486450.1:p.Ile309=
NM_000670.3:c.927T>A	NP_000661.2:p.Ile309=
NM_000670.4:c.927T>A	NP_000661.2:p.Ile309=
NM_001306171.1:c.984T>A	NP_001293100.1:p.Ile328=
NM_001306172.1:c.984T>A	NP_001293101.1:p.Ile328=
NR_037884.1:n.429-6294A>T
XR_938685.1:n.1155T>A
XR_938686.1:n.1146T>A
XR_938687.1:n.1019T>A
NM_000670.5:c.927T>A MANE Select	NP_000661.2:p.Ile309=
NM_001306171.2:c.984T>A	NP_001293100.1:p.Ile328=
NM_001306172.2:c.984T>A	NP_001293101.1:p.Ile328=