Canonical Allele Identifier: CA382902644

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118898449G>T (hg19) ; chr11:g.119027739G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027739G>T , CM000673.2:g.119027739G>T	GRCh38
NC_000011.9:g.118898449G>T , CM000673.1:g.118898449G>T	GRCh37
NC_000011.8:g.118403659G>T	NCBI36
NG_013331.1:g.8168C>A , LRG_187:g.8168C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.744C>A
ENST00000697845.1:n.668C>A
ENST00000697846.1:n.744C>A
ENST00000697847.1:n.744C>A
ENST00000697848.1:n.744C>A
ENST00000697849.1:n.1783C>A
ENST00000697850.1:n.744C>A
ENST00000697851.1:n.2104C>A
ENST00000638186.1:n.818C>A
ENST00000638360.1:n.650C>A
ENST00000638925.1:n.751C>A
ENST00000650539.1:n.920C>A
ENST00000330775.9:c.515C>A	ENSP00000476242.2:p.Ser172Tyr
ENST00000357590.9:c.515C>A	ENSP00000476176.2:p.Ser172Tyr
ENST00000524428.5:n.836C>A
ENST00000525039.5:n.938C>A
ENST00000525102.5:n.1272C>A
ENST00000525372.5:n.515C>A
ENST00000526275.5:n.1296C>A
ENST00000526626.6:n.477C>A
ENST00000527992.5:n.742C>A
ENST00000529510.5:n.399+455C>A
ENST00000530407.5:n.664C>A
ENST00000532085.1:n.3125C>A
ENST00000532888.6:n.810C>A
ENST00000538950.5:c.296C>A	ENSP00000475991.2:p.Ser99Tyr
ENST00000545985.5:c.515C>A	ENSP00000475241.2:p.Ser172Tyr
NM_001164277.1:c.515C>A , LRG_187t1:c.515C>A	NP_001157749.1:p.Ser172Tyr
NM_001164278.1:c.515C>A	NP_001157750.1:p.Ser172Tyr
NM_001164279.1:c.296C>A	NP_001157751.1:p.Ser99Tyr
NM_001164280.1:c.515C>A	NP_001157752.1:p.Ser172Tyr
NM_001467.5:c.515C>A	NP_001458.1:p.Ser172Tyr
NM_001164278.2:c.515C>A	NP_001157750.1:p.Ser172Tyr
NM_001164279.2:c.296C>A	NP_001157751.1:p.Ser99Tyr
NM_001164280.2:c.515C>A	NP_001157752.1:p.Ser172Tyr
NM_001467.6:c.515C>A	NP_001458.1:p.Ser172Tyr
NM_001164277.2:c.515C>A MANE Select	NP_001157749.1:p.Ser172Tyr