Canonical Allele Identifier: CA219340
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 68287
ClinVar RCV Id: RCV000059138
dbSNP Id: rs193302902

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027035A>G , CM000673.2:g.119027035A>G GRCh38
NC_000011.9:g.118897745A>G , CM000673.1:g.118897745A>G GRCh37
NC_000011.8:g.118402955A>G NCBI36
NG_013331.1:g.8871T>C , LRG_187:g.8871T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.916T>C
ENST00000697845.1:n.840T>C
ENST00000697846.1:n.916T>C
ENST00000697847.1:n.916T>C
ENST00000697848.1:n.916T>C
ENST00000697849.1:n.1955T>C
ENST00000697850.1:n.916T>C
ENST00000697851.1:n.2276T>C
ENST00000638186.1:n.990T>C
ENST00000638360.1:n.822T>C
ENST00000638925.1:n.923T>C
ENST00000650539.1:n.1092T>C
ENST00000330775.9:c.686T>C ENSP00000476242.2:p.Leu229Pro
ENST00000357590.9:c.686T>C ENSP00000476176.2:p.Leu229Pro
ENST00000524428.5:n.1008T>C
ENST00000525039.5:n.1110T>C
ENST00000525102.5:n.1444T>C
ENST00000525372.5:n.687T>C
ENST00000526275.5:n.1468T>C
ENST00000526626.6:n.649T>C
ENST00000527992.5:n.914T>C
ENST00000529510.5:n.460T>C
ENST00000530407.5:n.836T>C
ENST00000532085.1:n.3297T>C
ENST00000532888.6:n.982T>C
ENST00000538950.5:c.467T>C ENSP00000475991.2:p.Leu156Pro
ENST00000545985.5:c.686T>C ENSP00000475241.2:p.Leu229Pro
NM_001164277.1:c.686T>C , LRG_187t1:c.686T>C NP_001157749.1:p.Leu229Pro
NM_001164278.1:c.686T>C NP_001157750.1:p.Leu229Pro
NM_001164279.1:c.467T>C NP_001157751.1:p.Leu156Pro
NM_001164280.1:c.686T>C NP_001157752.1:p.Leu229Pro
NM_001467.5:c.686T>C NP_001458.1:p.Leu229Pro
NM_001164278.2:c.686T>C NP_001157750.1:p.Leu229Pro
NM_001164279.2:c.467T>C NP_001157751.1:p.Leu156Pro
NM_001164280.2:c.686T>C NP_001157752.1:p.Leu229Pro
NM_001467.6:c.686T>C NP_001458.1:p.Leu229Pro
NM_001164277.2:c.686T>C MANE Select NP_001157749.1:p.Leu229Pro