Canonical Allele Identifier: CA382901621

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897790T>C (hg19) ; chr11:g.119027080T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027080T>C , CM000673.2:g.119027080T>C	GRCh38
NC_000011.9:g.118897790T>C , CM000673.1:g.118897790T>C	GRCh37
NC_000011.8:g.118403000T>C	NCBI36
NG_013331.1:g.8826A>G , LRG_187:g.8826A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.871A>G
ENST00000697845.1:n.795A>G
ENST00000697846.1:n.871A>G
ENST00000697847.1:n.871A>G
ENST00000697848.1:n.871A>G
ENST00000697849.1:n.1910A>G
ENST00000697850.1:n.871A>G
ENST00000697851.1:n.2231A>G
ENST00000638186.1:n.945A>G
ENST00000638360.1:n.777A>G
ENST00000638925.1:n.878A>G
ENST00000650539.1:n.1047A>G
ENST00000330775.9:c.641A>G	ENSP00000476242.2:p.Glu214Gly
ENST00000357590.9:c.641A>G	ENSP00000476176.2:p.Glu214Gly
ENST00000524428.5:n.963A>G
ENST00000525039.5:n.1065A>G
ENST00000525102.5:n.1399A>G
ENST00000525372.5:n.642A>G
ENST00000526275.5:n.1423A>G
ENST00000526626.6:n.604A>G
ENST00000527992.5:n.869A>G
ENST00000529510.5:n.415A>G
ENST00000530407.5:n.791A>G
ENST00000532085.1:n.3252A>G
ENST00000532888.6:n.937A>G
ENST00000538950.5:c.422A>G	ENSP00000475991.2:p.Glu141Gly
ENST00000545985.5:c.641A>G	ENSP00000475241.2:p.Glu214Gly
NM_001164277.1:c.641A>G , LRG_187t1:c.641A>G	NP_001157749.1:p.Glu214Gly
NM_001164278.1:c.641A>G	NP_001157750.1:p.Glu214Gly
NM_001164279.1:c.422A>G	NP_001157751.1:p.Glu141Gly
NM_001164280.1:c.641A>G	NP_001157752.1:p.Glu214Gly
NM_001467.5:c.641A>G	NP_001458.1:p.Glu214Gly
NM_001164278.2:c.641A>G	NP_001157750.1:p.Glu214Gly
NM_001164279.2:c.422A>G	NP_001157751.1:p.Glu141Gly
NM_001164280.2:c.641A>G	NP_001157752.1:p.Glu214Gly
NM_001467.6:c.641A>G	NP_001458.1:p.Glu214Gly
NM_001164277.2:c.641A>G MANE Select	NP_001157749.1:p.Glu214Gly