Canonical Allele Identifier: CA357479815

Gene: ADH4

Linked Data

• dbSNP Id: rs1729129479
• MyVariant Identifiers: chr4:g.100048438C>G (hg19) ; chr4:g.99127287C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127287C>G , CM000666.2:g.99127287C>G	GRCh38
NC_000004.11:g.100048438C>G , CM000666.1:g.100048438C>G	GRCh37
NC_000004.10:g.100267461C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.901G>C MANE Select	ENSP00000265512.7:p.Ala301Pro
ENST00000265512.11:c.901G>C	ENSP00000265512.7:p.Ala301Pro
ENST00000505590.5:c.958G>C	ENSP00000425416.1:p.Ala320Pro
ENST00000506705.5:c.*875G>C	ENSP00000426667.1:n.*875G>C
ENST00000508393.5:c.958G>C	ENSP00000424630.1:p.Ala320Pro
ENST00000509471.5:c.334-555G>C	ENSP00000424583.1:n.334-555G>C
ENST00000629236.2:c.901G>C	ENSP00000486450.1:p.Ala301Pro
NM_000670.3:c.901G>C	NP_000661.2:p.Ala301Pro
NM_000670.4:c.901G>C	NP_000661.2:p.Ala301Pro
NM_001306171.1:c.958G>C	NP_001293100.1:p.Ala320Pro
NM_001306172.1:c.958G>C	NP_001293101.1:p.Ala320Pro
NR_037884.1:n.429-6268C>G
XR_938685.1:n.1129G>C
XR_938686.1:n.1120G>C
XR_938687.1:n.993G>C
NM_000670.5:c.901G>C MANE Select	NP_000661.2:p.Ala301Pro
NM_001306171.2:c.958G>C	NP_001293100.1:p.Ala320Pro
NM_001306172.2:c.958G>C	NP_001293101.1:p.Ala320Pro