Canonical Allele Identifier: CA477367721

Gene: SLC37A4

Linked Data

• ClinVar Variation Id: 558085
• ClinVar RCV Id: RCV000674308
• dbSNP Id: rs1300746467
• MyVariant Identifiers: chr11:g.118898411G>T (hg19) ; chr11:g.119027701G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027701G>T , CM000673.2:g.119027701G>T	GRCh38
NC_000011.9:g.118898411G>T , CM000673.1:g.118898411G>T	GRCh37
NC_000011.8:g.118403621G>T	NCBI36
NG_013331.1:g.8205C>A , LRG_187:g.8205C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.782C>A
ENST00000697845.1:n.706C>A
ENST00000697846.1:n.782C>A
ENST00000697847.1:n.782C>A
ENST00000697848.1:n.782C>A
ENST00000697849.1:n.1821C>A
ENST00000697850.1:n.782C>A
ENST00000697851.1:n.2142C>A
ENST00000638186.1:n.856C>A
ENST00000638360.1:n.688C>A
ENST00000638925.1:n.789C>A
ENST00000650539.1:n.958C>A
ENST00000330775.9:c.552C>A	ENSP00000476242.2:p.Leu184=
ENST00000357590.9:c.552C>A	ENSP00000476176.2:p.Leu184=
ENST00000524428.5:n.874C>A
ENST00000525039.5:n.976C>A
ENST00000525102.5:n.1310C>A
ENST00000525372.5:n.553C>A
ENST00000526275.5:n.1334C>A
ENST00000526626.6:n.515C>A
ENST00000527992.5:n.780C>A
ENST00000529510.5:n.399+493C>A
ENST00000530407.5:n.702C>A
ENST00000532085.1:n.3163C>A
ENST00000532888.6:n.848C>A
ENST00000538950.5:c.333C>A	ENSP00000475991.2:p.Leu111=
ENST00000545985.5:c.552C>A	ENSP00000475241.2:p.Leu184=
NM_001164277.1:c.552C>A , LRG_187t1:c.552C>A	NP_001157749.1:p.Leu184=
NM_001164278.1:c.552C>A	NP_001157750.1:p.Leu184=
NM_001164279.1:c.333C>A	NP_001157751.1:p.Leu111=
NM_001164280.1:c.552C>A	NP_001157752.1:p.Leu184=
NM_001467.5:c.552C>A	NP_001458.1:p.Leu184=
NM_001164278.2:c.552C>A	NP_001157750.1:p.Leu184=
NM_001164279.2:c.333C>A	NP_001157751.1:p.Leu111=
NM_001164280.2:c.552C>A	NP_001157752.1:p.Leu184=
NM_001467.6:c.552C>A	NP_001458.1:p.Leu184=
NM_001164277.2:c.552C>A MANE Select	NP_001157749.1:p.Leu184=