Canonical Allele Identifier: CA357479665

Gene: ADH4

Linked Data

• MyVariant Identifiers: chr4:g.100048366A>C (hg19) ; chr4:g.99127215A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127215A>C , CM000666.2:g.99127215A>C	GRCh38
NC_000004.11:g.100048366A>C , CM000666.1:g.100048366A>C	GRCh37
NC_000004.10:g.100267389A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.973T>G MANE Select	ENSP00000265512.7:p.Phe325Val
ENST00000265512.11:c.973T>G	ENSP00000265512.7:p.Phe325Val
ENST00000505590.5:c.1030T>G	ENSP00000425416.1:p.Phe344Val
ENST00000506705.5:c.*947T>G	ENSP00000426667.1:n.*947T>G
ENST00000508393.5:c.1030T>G	ENSP00000424630.1:p.Phe344Val
ENST00000509471.5:c.334-483T>G	ENSP00000424583.1:n.334-483T>G
ENST00000629236.2:c.973T>G	ENSP00000486450.1:p.Phe325Val
NM_000670.3:c.973T>G	NP_000661.2:p.Phe325Val
NM_000670.4:c.973T>G	NP_000661.2:p.Phe325Val
NM_001306171.1:c.1030T>G	NP_001293100.1:p.Phe344Val
NM_001306172.1:c.1030T>G	NP_001293101.1:p.Phe344Val
NR_037884.1:n.429-6340A>C
XR_938685.1:n.1201T>G
XR_938686.1:n.1192T>G
XR_938687.1:n.1065T>G
NM_000670.5:c.973T>G MANE Select	NP_000661.2:p.Phe325Val
NM_001306171.2:c.1030T>G	NP_001293100.1:p.Phe344Val
NM_001306172.2:c.1030T>G	NP_001293101.1:p.Phe344Val