Canonical Allele Identifier: CA382901638

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897793T>C (hg19) ; chr11:g.119027083T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027083T>C , CM000673.2:g.119027083T>C	GRCh38
NC_000011.9:g.118897793T>C , CM000673.1:g.118897793T>C	GRCh37
NC_000011.8:g.118403003T>C	NCBI36
NG_013331.1:g.8823A>G , LRG_187:g.8823A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.868A>G
ENST00000697845.1:n.792A>G
ENST00000697846.1:n.868A>G
ENST00000697847.1:n.868A>G
ENST00000697848.1:n.868A>G
ENST00000697849.1:n.1907A>G
ENST00000697850.1:n.868A>G
ENST00000697851.1:n.2228A>G
ENST00000638186.1:n.942A>G
ENST00000638360.1:n.774A>G
ENST00000638925.1:n.875A>G
ENST00000650539.1:n.1044A>G
ENST00000330775.9:c.638A>G	ENSP00000476242.2:p.Glu213Gly
ENST00000357590.9:c.638A>G	ENSP00000476176.2:p.Glu213Gly
ENST00000524428.5:n.960A>G
ENST00000525039.5:n.1062A>G
ENST00000525102.5:n.1396A>G
ENST00000525372.5:n.639A>G
ENST00000526275.5:n.1420A>G
ENST00000526626.6:n.601A>G
ENST00000527992.5:n.866A>G
ENST00000529510.5:n.412A>G
ENST00000530407.5:n.788A>G
ENST00000532085.1:n.3249A>G
ENST00000532888.6:n.934A>G
ENST00000538950.5:c.419A>G	ENSP00000475991.2:p.Glu140Gly
ENST00000545985.5:c.638A>G	ENSP00000475241.2:p.Glu213Gly
NM_001164277.1:c.638A>G , LRG_187t1:c.638A>G	NP_001157749.1:p.Glu213Gly
NM_001164278.1:c.638A>G	NP_001157750.1:p.Glu213Gly
NM_001164279.1:c.419A>G	NP_001157751.1:p.Glu140Gly
NM_001164280.1:c.638A>G	NP_001157752.1:p.Glu213Gly
NM_001467.5:c.638A>G	NP_001458.1:p.Glu213Gly
NM_001164278.2:c.638A>G	NP_001157750.1:p.Glu213Gly
NM_001164279.2:c.419A>G	NP_001157751.1:p.Glu140Gly
NM_001164280.2:c.638A>G	NP_001157752.1:p.Glu213Gly
NM_001467.6:c.638A>G	NP_001458.1:p.Glu213Gly
NM_001164277.2:c.638A>G MANE Select	NP_001157749.1:p.Glu213Gly