Canonical Allele Identifier: CA382902343

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118898422A>C (hg19) ; chr11:g.119027712A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027712A>C , CM000673.2:g.119027712A>C	GRCh38
NC_000011.9:g.118898422A>C , CM000673.1:g.118898422A>C	GRCh37
NC_000011.8:g.118403632A>C	NCBI36
NG_013331.1:g.8194T>G , LRG_187:g.8194T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.771T>G
ENST00000697845.1:n.695T>G
ENST00000697846.1:n.771T>G
ENST00000697847.1:n.771T>G
ENST00000697848.1:n.771T>G
ENST00000697849.1:n.1810T>G
ENST00000697850.1:n.771T>G
ENST00000697851.1:n.2131T>G
ENST00000638186.1:n.845T>G
ENST00000638360.1:n.677T>G
ENST00000638925.1:n.778T>G
ENST00000650539.1:n.947T>G
ENST00000330775.9:c.541T>G	ENSP00000476242.2:p.Phe181Val
ENST00000357590.9:c.541T>G	ENSP00000476176.2:p.Phe181Val
ENST00000524428.5:n.863T>G
ENST00000525039.5:n.965T>G
ENST00000525102.5:n.1299T>G
ENST00000525372.5:n.542T>G
ENST00000526275.5:n.1323T>G
ENST00000526626.6:n.504T>G
ENST00000527992.5:n.769T>G
ENST00000529510.5:n.399+482T>G
ENST00000530407.5:n.691T>G
ENST00000532085.1:n.3152T>G
ENST00000532888.6:n.837T>G
ENST00000538950.5:c.322T>G	ENSP00000475991.2:p.Phe108Val
ENST00000545985.5:c.541T>G	ENSP00000475241.2:p.Phe181Val
NM_001164277.1:c.541T>G , LRG_187t1:c.541T>G	NP_001157749.1:p.Phe181Val
NM_001164278.1:c.541T>G	NP_001157750.1:p.Phe181Val
NM_001164279.1:c.322T>G	NP_001157751.1:p.Phe108Val
NM_001164280.1:c.541T>G	NP_001157752.1:p.Phe181Val
NM_001467.5:c.541T>G	NP_001458.1:p.Phe181Val
NM_001164278.2:c.541T>G	NP_001157750.1:p.Phe181Val
NM_001164279.2:c.322T>G	NP_001157751.1:p.Phe108Val
NM_001164280.2:c.541T>G	NP_001157752.1:p.Phe181Val
NM_001467.6:c.541T>G	NP_001458.1:p.Phe181Val
NM_001164277.2:c.541T>G MANE Select	NP_001157749.1:p.Phe181Val