Canonical Allele Identifier: CA440304726

Gene: ADH4

Linked Data

• MyVariant Identifiers: chr4:g.100048382A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127231A>C , CM000666.2:g.99127231A>C	GRCh38
NC_000004.11:g.100048382A>C , CM000666.1:g.100048382A>C	GRCh37
NC_000004.10:g.100267405A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.957T>G MANE Select	ENSP00000265512.7:p.Thr319=
ENST00000265512.11:c.957T>G	ENSP00000265512.7:p.Thr319=
ENST00000505590.5:c.1014T>G	ENSP00000425416.1:p.Thr338=
ENST00000506705.5:c.*931T>G	ENSP00000426667.1:n.*931T>G
ENST00000508393.5:c.1014T>G	ENSP00000424630.1:p.Thr338=
ENST00000509471.5:c.334-499T>G	ENSP00000424583.1:n.334-499T>G
ENST00000629236.2:c.957T>G	ENSP00000486450.1:p.Thr319=
NM_000670.3:c.957T>G	NP_000661.2:p.Thr319=
NM_000670.4:c.957T>G	NP_000661.2:p.Thr319=
NM_001306171.1:c.1014T>G	NP_001293100.1:p.Thr338=
NM_001306172.1:c.1014T>G	NP_001293101.1:p.Thr338=
NR_037884.1:n.429-6324A>C
XR_938685.1:n.1185T>G
XR_938686.1:n.1176T>G
XR_938687.1:n.1049T>G
NM_000670.5:c.957T>G MANE Select	NP_000661.2:p.Thr319=
NM_001306171.2:c.1014T>G	NP_001293100.1:p.Thr338=
NM_001306172.2:c.1014T>G	NP_001293101.1:p.Thr338=