Canonical Allele Identifier: CA382897155

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118896687T>C (hg19) ; chr11:g.119025977T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025977T>C , CM000673.2:g.119025977T>C	GRCh38
NC_000011.9:g.118896687T>C , CM000673.1:g.118896687T>C	GRCh37
NC_000011.8:g.118401897T>C	NCBI36
NG_013331.1:g.9929A>G , LRG_187:g.9929A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1118A>G
ENST00000697845.1:n.1898A>G
ENST00000697846.1:n.1118A>G
ENST00000697847.1:n.1202-220A>G
ENST00000697848.1:n.1204A>G
ENST00000697849.1:n.3013A>G
ENST00000697850.1:n.1204A>G
ENST00000697851.1:n.2812A>G
ENST00000638186.1:n.1278A>G
ENST00000638360.1:n.1110A>G
ENST00000638925.1:n.1243A>G
ENST00000650539.1:n.1380A>G
ENST00000330775.9:c.974A>G	ENSP00000476242.2:p.Asp325Gly
ENST00000357590.9:c.974A>G	ENSP00000476176.2:p.Asp325Gly
ENST00000524428.5:n.1210A>G
ENST00000525039.5:n.1398A>G
ENST00000525102.5:n.1732A>G
ENST00000525372.5:n.1072A>G
ENST00000526275.5:n.1756A>G
ENST00000527992.5:n.1202A>G
ENST00000529510.5:n.662A>G
ENST00000530407.5:n.1124A>G
ENST00000532085.1:n.4355A>G
ENST00000538950.5:c.755A>G	ENSP00000475991.2:p.Asp252Gly
ENST00000545985.5:c.974A>G	ENSP00000475241.2:p.Asp325Gly
NM_001164277.1:c.974A>G , LRG_187t1:c.974A>G	NP_001157749.1:p.Asp325Gly
NM_001164278.1:c.974A>G	NP_001157750.1:p.Asp325Gly
NM_001164279.1:c.755A>G	NP_001157751.1:p.Asp252Gly
NM_001164280.1:c.974A>G	NP_001157752.1:p.Asp325Gly
NM_001467.5:c.974A>G	NP_001458.1:p.Asp325Gly
NM_001164278.2:c.974A>G	NP_001157750.1:p.Asp325Gly
NM_001164279.2:c.755A>G	NP_001157751.1:p.Asp252Gly
NM_001164280.2:c.974A>G	NP_001157752.1:p.Asp325Gly
NM_001467.6:c.974A>G	NP_001458.1:p.Asp325Gly
NM_001164277.2:c.974A>G MANE Select	NP_001157749.1:p.Asp325Gly