Canonical Allele Identifier: CA3018665

Gene: ADH4

Linked Data

• dbSNP Id: rs767318009
• ExAC: 4:100048457 T / C
• gnomAD v2: 4-100048457-T-C
• gnomAD v4: 4-99127306-T-C
• MyVariant Identifiers: chr4:g.100048457T>C (hg19) ; chr4:g.99127306T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127306T>C , CM000666.2:g.99127306T>C	GRCh38
NC_000004.11:g.100048457T>C , CM000666.1:g.100048457T>C	GRCh37
NC_000004.10:g.100267480T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.882A>G MANE Select	ENSP00000265512.7:p.Ser294=
ENST00000265512.11:c.882A>G	ENSP00000265512.7:p.Ser294=
ENST00000505590.5:c.939A>G	ENSP00000425416.1:p.Ser313=
ENST00000506705.5:c.*856A>G	ENSP00000426667.1:n.*856A>G
ENST00000508393.5:c.939A>G	ENSP00000424630.1:p.Ser313=
ENST00000509471.5:c.334-574A>G	ENSP00000424583.1:n.334-574A>G
ENST00000629236.2:c.882A>G	ENSP00000486450.1:p.Ser294=
NM_000670.3:c.882A>G	NP_000661.2:p.Ser294=
NM_000670.4:c.882A>G	NP_000661.2:p.Ser294=
NM_001306171.1:c.939A>G	NP_001293100.1:p.Ser313=
NM_001306172.1:c.939A>G	NP_001293101.1:p.Ser313=
NR_037884.1:n.429-6249T>C
XR_938685.1:n.1110A>G
XR_938686.1:n.1101A>G
XR_938687.1:n.974A>G
NM_000670.5:c.882A>G MANE Select	NP_000661.2:p.Ser294=
NM_001306171.2:c.939A>G	NP_001293100.1:p.Ser313=
NM_001306172.2:c.939A>G	NP_001293101.1:p.Ser313=