Canonical Allele Identifier: CA477367212

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1943610559
• MyVariant Identifiers: chr11:g.118898345G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027635G>C , CM000673.2:g.119027635G>C	GRCh38
NC_000011.9:g.118898345G>C , CM000673.1:g.118898345G>C	GRCh37
NC_000011.8:g.118403555G>C	NCBI36
NG_013331.1:g.8271C>G , LRG_187:g.8271C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.848C>G
ENST00000697845.1:n.772C>G
ENST00000697846.1:n.848C>G
ENST00000697847.1:n.848C>G
ENST00000697848.1:n.848C>G
ENST00000697849.1:n.1887C>G
ENST00000697850.1:n.848C>G
ENST00000697851.1:n.2208C>G
ENST00000638186.1:n.922C>G
ENST00000638360.1:n.754C>G
ENST00000638925.1:n.855C>G
ENST00000650539.1:n.1024C>G
ENST00000330775.9:c.618C>G	ENSP00000476242.2:p.Gly206=
ENST00000357590.9:c.618C>G	ENSP00000476176.2:p.Gly206=
ENST00000524428.5:n.940C>G
ENST00000525039.5:n.1042C>G
ENST00000525102.5:n.1376C>G
ENST00000525372.5:n.619C>G
ENST00000526275.5:n.1400C>G
ENST00000526626.6:n.581C>G
ENST00000527992.5:n.846C>G
ENST00000529510.5:n.400-540C>G
ENST00000530407.5:n.768C>G
ENST00000532085.1:n.3229C>G
ENST00000532888.6:n.914C>G
ENST00000538950.5:c.399C>G	ENSP00000475991.2:p.Gly133=
ENST00000545985.5:c.618C>G	ENSP00000475241.2:p.Gly206=
NM_001164277.1:c.618C>G , LRG_187t1:c.618C>G	NP_001157749.1:p.Gly206=
NM_001164278.1:c.618C>G	NP_001157750.1:p.Gly206=
NM_001164279.1:c.399C>G	NP_001157751.1:p.Gly133=
NM_001164280.1:c.618C>G	NP_001157752.1:p.Gly206=
NM_001467.5:c.618C>G	NP_001458.1:p.Gly206=
NM_001164278.2:c.618C>G	NP_001157750.1:p.Gly206=
NM_001164279.2:c.399C>G	NP_001157751.1:p.Gly133=
NM_001164280.2:c.618C>G	NP_001157752.1:p.Gly206=
NM_001467.6:c.618C>G	NP_001458.1:p.Gly206=
NM_001164277.2:c.618C>G MANE Select	NP_001157749.1:p.Gly206=