Canonical Allele Identifier: CA382901573

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897779G>C (hg19) ; chr11:g.119027069G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027069G>C , CM000673.2:g.119027069G>C	GRCh38
NC_000011.9:g.118897779G>C , CM000673.1:g.118897779G>C	GRCh37
NC_000011.8:g.118402989G>C	NCBI36
NG_013331.1:g.8837C>G , LRG_187:g.8837C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.882C>G
ENST00000697845.1:n.806C>G
ENST00000697846.1:n.882C>G
ENST00000697847.1:n.882C>G
ENST00000697848.1:n.882C>G
ENST00000697849.1:n.1921C>G
ENST00000697850.1:n.882C>G
ENST00000697851.1:n.2242C>G
ENST00000638186.1:n.956C>G
ENST00000638360.1:n.788C>G
ENST00000638925.1:n.889C>G
ENST00000650539.1:n.1058C>G
ENST00000330775.9:c.652C>G	ENSP00000476242.2:p.Gln218Glu
ENST00000357590.9:c.652C>G	ENSP00000476176.2:p.Gln218Glu
ENST00000524428.5:n.974C>G
ENST00000525039.5:n.1076C>G
ENST00000525102.5:n.1410C>G
ENST00000525372.5:n.653C>G
ENST00000526275.5:n.1434C>G
ENST00000526626.6:n.615C>G
ENST00000527992.5:n.880C>G
ENST00000529510.5:n.426C>G
ENST00000530407.5:n.802C>G
ENST00000532085.1:n.3263C>G
ENST00000532888.6:n.948C>G
ENST00000538950.5:c.433C>G	ENSP00000475991.2:p.Gln145Glu
ENST00000545985.5:c.652C>G	ENSP00000475241.2:p.Gln218Glu
NM_001164277.1:c.652C>G , LRG_187t1:c.652C>G	NP_001157749.1:p.Gln218Glu
NM_001164278.1:c.652C>G	NP_001157750.1:p.Gln218Glu
NM_001164279.1:c.433C>G	NP_001157751.1:p.Gln145Glu
NM_001164280.1:c.652C>G	NP_001157752.1:p.Gln218Glu
NM_001467.5:c.652C>G	NP_001458.1:p.Gln218Glu
NM_001164278.2:c.652C>G	NP_001157750.1:p.Gln218Glu
NM_001164279.2:c.433C>G	NP_001157751.1:p.Gln145Glu
NM_001164280.2:c.652C>G	NP_001157752.1:p.Gln218Glu
NM_001467.6:c.652C>G	NP_001458.1:p.Gln218Glu
NM_001164277.2:c.652C>G MANE Select	NP_001157749.1:p.Gln218Glu