Canonical Allele Identifier: CA357480213

Gene: ADH4

Linked Data

• MyVariant Identifiers: chr4:g.100048489C>T (hg19) ; chr4:g.99127338C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127338C>T , CM000666.2:g.99127338C>T	GRCh38
NC_000004.11:g.100048489C>T , CM000666.1:g.100048489C>T	GRCh37
NC_000004.10:g.100267512C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.850G>A MANE Select	ENSP00000265512.7:p.Ala284Thr
ENST00000265512.11:c.850G>A	ENSP00000265512.7:p.Ala284Thr
ENST00000505590.5:c.907G>A	ENSP00000425416.1:p.Ala303Thr
ENST00000506705.5:c.*824G>A	ENSP00000426667.1:n.*824G>A
ENST00000508393.5:c.907G>A	ENSP00000424630.1:p.Ala303Thr
ENST00000509471.5:c.334-606G>A	ENSP00000424583.1:n.334-606G>A
ENST00000629236.2:c.850G>A	ENSP00000486450.1:p.Ala284Thr
NM_000670.3:c.850G>A	NP_000661.2:p.Ala284Thr
NM_000670.4:c.850G>A	NP_000661.2:p.Ala284Thr
NM_001306171.1:c.907G>A	NP_001293100.1:p.Ala303Thr
NM_001306172.1:c.907G>A	NP_001293101.1:p.Ala303Thr
NR_037884.1:n.429-6217C>T
XR_938685.1:n.1078G>A
XR_938686.1:n.1069G>A
XR_938687.1:n.942G>A
NM_000670.5:c.850G>A MANE Select	NP_000661.2:p.Ala284Thr
NM_001306171.2:c.907G>A	NP_001293100.1:p.Ala303Thr
NM_001306172.2:c.907G>A	NP_001293101.1:p.Ala303Thr