Canonical Allele Identifier: CA382903117

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1180944825
• gnomAD v2: 11-118898486-C-T
• gnomAD v4: 11-119027776-C-T
• MyVariant Identifiers: chr11:g.118898486C>T (hg19) ; chr11:g.119027776C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027776C>T , CM000673.2:g.119027776C>T	GRCh38
NC_000011.9:g.118898486C>T , CM000673.1:g.118898486C>T	GRCh37
NC_000011.8:g.118403696C>T	NCBI36
NG_013331.1:g.8131G>A , LRG_187:g.8131G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.707G>A
ENST00000697845.1:n.631G>A
ENST00000697846.1:n.707G>A
ENST00000697847.1:n.707G>A
ENST00000697848.1:n.707G>A
ENST00000697849.1:n.1746G>A
ENST00000697850.1:n.707G>A
ENST00000697851.1:n.2067G>A
ENST00000638186.1:n.781G>A
ENST00000638360.1:n.619-6G>A
ENST00000638925.1:n.714G>A
ENST00000650539.1:n.883G>A
ENST00000330775.9:c.478G>A	ENSP00000476242.2:p.Ala160Thr
ENST00000357590.9:c.478G>A	ENSP00000476176.2:p.Ala160Thr
ENST00000524428.5:n.799G>A
ENST00000525039.5:n.901G>A
ENST00000525102.5:n.1235G>A
ENST00000525372.5:n.478G>A
ENST00000526275.5:n.1259G>A
ENST00000526626.6:n.440G>A
ENST00000527992.5:n.705G>A
ENST00000529510.5:n.399+418G>A
ENST00000530407.5:n.627G>A
ENST00000532085.1:n.3088G>A
ENST00000532888.6:n.773G>A
ENST00000538950.5:c.259G>A	ENSP00000475991.2:p.Ala87Thr
ENST00000545985.5:c.478G>A	ENSP00000475241.2:p.Ala160Thr
NM_001164277.1:c.478G>A , LRG_187t1:c.478G>A	NP_001157749.1:p.Ala160Thr
NM_001164278.1:c.478G>A	NP_001157750.1:p.Ala160Thr
NM_001164279.1:c.259G>A	NP_001157751.1:p.Ala87Thr
NM_001164280.1:c.478G>A	NP_001157752.1:p.Ala160Thr
NM_001467.5:c.478G>A	NP_001458.1:p.Ala160Thr
NM_001164278.2:c.478G>A	NP_001157750.1:p.Ala160Thr
NM_001164279.2:c.259G>A	NP_001157751.1:p.Ala87Thr
NM_001164280.2:c.478G>A	NP_001157752.1:p.Ala160Thr
NM_001467.6:c.478G>A	NP_001458.1:p.Ala160Thr
NM_001164277.2:c.478G>A MANE Select	NP_001157749.1:p.Ala160Thr