Canonical Allele Identifier: CA382898192

Gene: SLC37A4

Linked Data

• ClinVar Variation Id: 553477
• ClinVar RCV Id: RCV000668942
• dbSNP Id: rs1320796917
• MyVariant Identifiers: chr11:g.118896787C>G (hg19) ; chr11:g.119026077C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026077C>G , CM000673.2:g.119026077C>G	GRCh38
NC_000011.9:g.118896787C>G , CM000673.1:g.118896787C>G	GRCh37
NC_000011.8:g.118401997C>G	NCBI36
NG_013331.1:g.9829G>C , LRG_187:g.9829G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1018G>C
ENST00000697845.1:n.1798G>C
ENST00000697846.1:n.1018G>C
ENST00000697847.1:n.1202-320G>C
ENST00000697848.1:n.1104G>C
ENST00000697849.1:n.2913G>C
ENST00000697850.1:n.1104G>C
ENST00000697851.1:n.2712G>C
ENST00000638186.1:n.1178G>C
ENST00000638360.1:n.1010G>C
ENST00000638925.1:n.1143G>C
ENST00000650539.1:n.1280G>C
ENST00000330775.9:c.874G>C	ENSP00000476242.2:p.Gly292Arg
ENST00000357590.9:c.874G>C	ENSP00000476176.2:p.Gly292Arg
ENST00000524428.5:n.1110G>C
ENST00000525039.5:n.1298G>C
ENST00000525102.5:n.1632G>C
ENST00000525372.5:n.972G>C
ENST00000526275.5:n.1656G>C
ENST00000527992.5:n.1102G>C
ENST00000529510.5:n.562G>C
ENST00000530407.5:n.1024G>C
ENST00000532085.1:n.4255G>C
ENST00000538950.5:c.655G>C	ENSP00000475991.2:p.Gly219Arg
ENST00000545985.5:c.874G>C	ENSP00000475241.2:p.Gly292Arg
NM_001164277.1:c.874G>C , LRG_187t1:c.874G>C	NP_001157749.1:p.Gly292Arg
NM_001164278.1:c.874G>C	NP_001157750.1:p.Gly292Arg
NM_001164279.1:c.655G>C	NP_001157751.1:p.Gly219Arg
NM_001164280.1:c.874G>C	NP_001157752.1:p.Gly292Arg
NM_001467.5:c.874G>C	NP_001458.1:p.Gly292Arg
NM_001164278.2:c.874G>C	NP_001157750.1:p.Gly292Arg
NM_001164279.2:c.655G>C	NP_001157751.1:p.Gly219Arg
NM_001164280.2:c.874G>C	NP_001157752.1:p.Gly292Arg
NM_001467.6:c.874G>C	NP_001458.1:p.Gly292Arg
NM_001164277.2:c.874G>C MANE Select	NP_001157749.1:p.Gly292Arg