Canonical Allele Identifier: CA602577673
Gene: SLC37A4 HGNC NCBI

Linked Data

dbSNP Id: rs1194259722

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027771_119027772del , CM000673.2:g.119027771_119027772del GRCh38
NC_000011.9:g.118898481_118898482del , CM000673.1:g.118898481_118898482del GRCh37
NC_000011.8:g.118403691_118403692del NCBI36
NG_013331.1:g.8137_8138del , LRG_187:g.8137_8138del

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.713_714del
ENST00000697845.1:n.637_638del
ENST00000697846.1:n.713_714del
ENST00000697847.1:n.713_714del
ENST00000697848.1:n.713_714del
ENST00000697849.1:n.1752_1753del
ENST00000697850.1:n.713_714del
ENST00000697851.1:n.2073_2074del
ENST00000638186.1:n.787_788del
ENST00000638360.1:n.619_620del
ENST00000638925.1:n.720_721del
ENST00000650539.1:n.889_890del
ENST00000330775.9:c.484_485del ENSP00000476242.2:p.Ser162LeufsTer28
ENST00000357590.9:c.484_485del ENSP00000476176.2:p.Ser162LeufsTer28
ENST00000524428.5:n.805_806del
ENST00000525039.5:n.907_908del
ENST00000525102.5:n.1241_1242del
ENST00000525372.5:n.484_485del
ENST00000526275.5:n.1265_1266del
ENST00000526626.6:n.446_447del
ENST00000527992.5:n.711_712del
ENST00000529510.5:n.399+424_399+425del
ENST00000530407.5:n.633_634del
ENST00000532085.1:n.3094_3095del
ENST00000532888.6:n.779_780del
ENST00000538950.5:c.265_266del ENSP00000475991.2:p.Ser89LeufsTer28
ENST00000545985.5:c.484_485del ENSP00000475241.2:p.Ser162LeufsTer28
NM_001164277.1:c.484_485del , LRG_187t1:c.484_485del NP_001157749.1:p.Ser162LeufsTer28
NM_001164278.1:c.484_485del NP_001157750.1:p.Ser162LeufsTer28
NM_001164279.1:c.265_266del NP_001157751.1:p.Ser89LeufsTer28
NM_001164280.1:c.484_485del NP_001157752.1:p.Ser162LeufsTer28
NM_001467.5:c.484_485del NP_001458.1:p.Ser162LeufsTer28
NM_001164278.2:c.484_485del NP_001157750.1:p.Ser162LeufsTer28
NM_001164279.2:c.265_266del NP_001157751.1:p.Ser89LeufsTer28
NM_001164280.2:c.484_485del NP_001157752.1:p.Ser162LeufsTer28
NM_001467.6:c.484_485del NP_001458.1:p.Ser162LeufsTer28
NM_001164277.2:c.484_485del MANE Select NP_001157749.1:p.Ser162LeufsTer28