Canonical Allele Identifier: CA382901463

Gene: SLC37A4

Linked Data

• ClinVar Variation Id: 557319
• ClinVar RCV Id: RCV000673445
• dbSNP Id: rs1555191101
• MyVariant Identifiers: chr11:g.118897751C>G (hg19) ; chr11:g.119027041C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027041C>G , CM000673.2:g.119027041C>G	GRCh38
NC_000011.9:g.118897751C>G , CM000673.1:g.118897751C>G	GRCh37
NC_000011.8:g.118402961C>G	NCBI36
NG_013331.1:g.8865G>C , LRG_187:g.8865G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.910G>C
ENST00000697845.1:n.834G>C
ENST00000697846.1:n.910G>C
ENST00000697847.1:n.910G>C
ENST00000697848.1:n.910G>C
ENST00000697849.1:n.1949G>C
ENST00000697850.1:n.910G>C
ENST00000697851.1:n.2270G>C
ENST00000638186.1:n.984G>C
ENST00000638360.1:n.816G>C
ENST00000638925.1:n.917G>C
ENST00000650539.1:n.1086G>C
ENST00000330775.9:c.680G>C	ENSP00000476242.2:p.Trp227Ser
ENST00000357590.9:c.680G>C	ENSP00000476176.2:p.Trp227Ser
ENST00000524428.5:n.1002G>C
ENST00000525039.5:n.1104G>C
ENST00000525102.5:n.1438G>C
ENST00000525372.5:n.681G>C
ENST00000526275.5:n.1462G>C
ENST00000526626.6:n.643G>C
ENST00000527992.5:n.908G>C
ENST00000529510.5:n.454G>C
ENST00000530407.5:n.830G>C
ENST00000532085.1:n.3291G>C
ENST00000532888.6:n.976G>C
ENST00000538950.5:c.461G>C	ENSP00000475991.2:p.Trp154Ser
ENST00000545985.5:c.680G>C	ENSP00000475241.2:p.Trp227Ser
NM_001164277.1:c.680G>C , LRG_187t1:c.680G>C	NP_001157749.1:p.Trp227Ser
NM_001164278.1:c.680G>C	NP_001157750.1:p.Trp227Ser
NM_001164279.1:c.461G>C	NP_001157751.1:p.Trp154Ser
NM_001164280.1:c.680G>C	NP_001157752.1:p.Trp227Ser
NM_001467.5:c.680G>C	NP_001458.1:p.Trp227Ser
NM_001164278.2:c.680G>C	NP_001157750.1:p.Trp227Ser
NM_001164279.2:c.461G>C	NP_001157751.1:p.Trp154Ser
NM_001164280.2:c.680G>C	NP_001157752.1:p.Trp227Ser
NM_001467.6:c.680G>C	NP_001458.1:p.Trp227Ser
NM_001164277.2:c.680G>C MANE Select	NP_001157749.1:p.Trp227Ser