Canonical Allele Identifier: CA382897602

Gene: SLC37A4

Linked Data

• ClinVar Variation Id: 555977
• ClinVar RCV Id: RCV000671902
• dbSNP Id: rs1555190726
• MyVariant Identifiers: chr11:g.118896724C>T (hg19) ; chr11:g.119026014C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026014C>T , CM000673.2:g.119026014C>T	GRCh38
NC_000011.9:g.118896724C>T , CM000673.1:g.118896724C>T	GRCh37
NC_000011.8:g.118401934C>T	NCBI36
NG_013331.1:g.9892G>A , LRG_187:g.9892G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1081G>A
ENST00000697845.1:n.1861G>A
ENST00000697846.1:n.1081G>A
ENST00000697847.1:n.1202-257G>A
ENST00000697848.1:n.1167G>A
ENST00000697849.1:n.2976G>A
ENST00000697850.1:n.1167G>A
ENST00000697851.1:n.2775G>A
ENST00000638186.1:n.1241G>A
ENST00000638360.1:n.1073G>A
ENST00000638925.1:n.1206G>A
ENST00000650539.1:n.1343G>A
ENST00000330775.9:c.937G>A	ENSP00000476242.2:p.Val313Met
ENST00000357590.9:c.937G>A	ENSP00000476176.2:p.Val313Met
ENST00000524428.5:n.1173G>A
ENST00000525039.5:n.1361G>A
ENST00000525102.5:n.1695G>A
ENST00000525372.5:n.1035G>A
ENST00000526275.5:n.1719G>A
ENST00000527992.5:n.1165G>A
ENST00000529510.5:n.625G>A
ENST00000530407.5:n.1087G>A
ENST00000532085.1:n.4318G>A
ENST00000538950.5:c.718G>A	ENSP00000475991.2:p.Val240Met
ENST00000545985.5:c.937G>A	ENSP00000475241.2:p.Val313Met
NM_001164277.1:c.937G>A , LRG_187t1:c.937G>A	NP_001157749.1:p.Val313Met
NM_001164278.1:c.937G>A	NP_001157750.1:p.Val313Met
NM_001164279.1:c.718G>A	NP_001157751.1:p.Val240Met
NM_001164280.1:c.937G>A	NP_001157752.1:p.Val313Met
NM_001467.5:c.937G>A	NP_001458.1:p.Val313Met
NM_001164278.2:c.937G>A	NP_001157750.1:p.Val313Met
NM_001164279.2:c.718G>A	NP_001157751.1:p.Val240Met
NM_001164280.2:c.937G>A	NP_001157752.1:p.Val313Met
NM_001467.6:c.937G>A	NP_001458.1:p.Val313Met
NM_001164277.2:c.937G>A MANE Select	NP_001157749.1:p.Val313Met