Canonical Allele Identifier: CA357479801

Gene: ADH4

Linked Data

• MyVariant Identifiers: chr4:g.100048431C>G (hg19) ; chr4:g.99127280C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127280C>G , CM000666.2:g.99127280C>G	GRCh38
NC_000004.11:g.100048431C>G , CM000666.1:g.100048431C>G	GRCh37
NC_000004.10:g.100267454C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.908G>C MANE Select	ENSP00000265512.7:p.Gly303Ala
ENST00000265512.11:c.908G>C	ENSP00000265512.7:p.Gly303Ala
ENST00000505590.5:c.965G>C	ENSP00000425416.1:p.Gly322Ala
ENST00000506705.5:c.*882G>C	ENSP00000426667.1:n.*882G>C
ENST00000508393.5:c.965G>C	ENSP00000424630.1:p.Gly322Ala
ENST00000509471.5:c.334-548G>C	ENSP00000424583.1:n.334-548G>C
ENST00000629236.2:c.908G>C	ENSP00000486450.1:p.Gly303Ala
NM_000670.3:c.908G>C	NP_000661.2:p.Gly303Ala
NM_000670.4:c.908G>C	NP_000661.2:p.Gly303Ala
NM_001306171.1:c.965G>C	NP_001293100.1:p.Gly322Ala
NM_001306172.1:c.965G>C	NP_001293101.1:p.Gly322Ala
NR_037884.1:n.429-6275C>G
XR_938685.1:n.1136G>C
XR_938686.1:n.1127G>C
XR_938687.1:n.1000G>C
NM_000670.5:c.908G>C MANE Select	NP_000661.2:p.Gly303Ala
NM_001306171.2:c.965G>C	NP_001293100.1:p.Gly322Ala
NM_001306172.2:c.965G>C	NP_001293101.1:p.Gly322Ala