Canonical Allele Identifier: CA382902442

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1428216442
• gnomAD v3: 11-119027721-C-T
• gnomAD v4: 11-119027721-C-T
• MyVariant Identifiers: chr11:g.118898431C>T (hg19) ; chr11:g.119027721C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027721C>T , CM000673.2:g.119027721C>T	GRCh38
NC_000011.9:g.118898431C>T , CM000673.1:g.118898431C>T	GRCh37
NC_000011.8:g.118403641C>T	NCBI36
NG_013331.1:g.8185G>A , LRG_187:g.8185G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.762G>A
ENST00000697845.1:n.686G>A
ENST00000697846.1:n.762G>A
ENST00000697847.1:n.762G>A
ENST00000697848.1:n.762G>A
ENST00000697849.1:n.1801G>A
ENST00000697850.1:n.762G>A
ENST00000697851.1:n.2122G>A
ENST00000638186.1:n.836G>A
ENST00000638360.1:n.668G>A
ENST00000638925.1:n.769G>A
ENST00000650539.1:n.938G>A
ENST00000330775.9:c.532G>A	ENSP00000476242.2:p.Val178Ile
ENST00000357590.9:c.532G>A	ENSP00000476176.2:p.Val178Ile
ENST00000524428.5:n.854G>A
ENST00000525039.5:n.956G>A
ENST00000525102.5:n.1290G>A
ENST00000525372.5:n.533G>A
ENST00000526275.5:n.1314G>A
ENST00000526626.6:n.495G>A
ENST00000527992.5:n.760G>A
ENST00000529510.5:n.399+473G>A
ENST00000530407.5:n.682G>A
ENST00000532085.1:n.3143G>A
ENST00000532888.6:n.828G>A
ENST00000538950.5:c.313G>A	ENSP00000475991.2:p.Val105Ile
ENST00000545985.5:c.532G>A	ENSP00000475241.2:p.Val178Ile
NM_001164277.1:c.532G>A , LRG_187t1:c.532G>A	NP_001157749.1:p.Val178Ile
NM_001164278.1:c.532G>A	NP_001157750.1:p.Val178Ile
NM_001164279.1:c.313G>A	NP_001157751.1:p.Val105Ile
NM_001164280.1:c.532G>A	NP_001157752.1:p.Val178Ile
NM_001467.5:c.532G>A	NP_001458.1:p.Val178Ile
NM_001164278.2:c.532G>A	NP_001157750.1:p.Val178Ile
NM_001164279.2:c.313G>A	NP_001157751.1:p.Val105Ile
NM_001164280.2:c.532G>A	NP_001157752.1:p.Val178Ile
NM_001467.6:c.532G>A	NP_001458.1:p.Val178Ile
NM_001164277.2:c.532G>A MANE Select	NP_001157749.1:p.Val178Ile