Canonical Allele Identifier: CA2003749726
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027768_119027770delinsGCT , CM000673.2:g.119027768_119027770delinsGCT GRCh38
NC_000011.9:g.118898478_118898480delinsGCT , CM000673.1:g.118898478_118898480delinsGCT GRCh37
NC_000011.8:g.118403688_118403690delinsGCT NCBI36
NG_013331.1:g.8137_8139delinsAGC , LRG_187:g.8137_8139delinsAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.713_715delinsAGC
ENST00000697845.1:n.637_639delinsAGC
ENST00000697846.1:n.713_715delinsAGC
ENST00000697847.1:n.713_715delinsAGC
ENST00000697848.1:n.713_715delinsAGC
ENST00000697849.1:n.1752_1754delinsAGC
ENST00000697850.1:n.713_715delinsAGC
ENST00000697851.1:n.2073_2075delinsAGC
ENST00000638186.1:n.787_789delinsAGC
ENST00000638360.1:n.619_621delinsAGC
ENST00000638925.1:n.720_722delinsAGC
ENST00000650539.1:n.889_891delinsAGC
ENST00000330775.9:c.484_486delinsAGC ENSP00000476242.2:p.Ser162=
ENST00000357590.9:c.484_486delinsAGC ENSP00000476176.2:p.Ser162=
ENST00000524428.5:n.805_807delinsAGC
ENST00000525039.5:n.907_909delinsAGC
ENST00000525102.5:n.1241_1243delinsAGC
ENST00000525372.5:n.484_486delinsAGC
ENST00000526275.5:n.1265_1267delinsAGC
ENST00000526626.6:n.446_448delinsAGC
ENST00000527992.5:n.711_713delinsAGC
ENST00000529510.5:n.399+424_399+426delinsAGC
ENST00000530407.5:n.633_635delinsAGC
ENST00000532085.1:n.3094_3096delinsAGC
ENST00000532888.6:n.779_781delinsAGC
ENST00000538950.5:c.265_267delinsAGC ENSP00000475991.2:p.Ser89=
ENST00000545985.5:c.484_486delinsAGC ENSP00000475241.2:p.Ser162=
NM_001164277.1:c.484_486delinsAGC , LRG_187t1:c.484_486delinsAGC NP_001157749.1:p.Ser162=
NM_001164278.1:c.484_486delinsAGC NP_001157750.1:p.Ser162=
NM_001164279.1:c.265_267delinsAGC NP_001157751.1:p.Ser89=
NM_001164280.1:c.484_486delinsAGC NP_001157752.1:p.Ser162=
NM_001467.5:c.484_486delinsAGC NP_001458.1:p.Ser162=
NM_001164278.2:c.484_486delinsAGC NP_001157750.1:p.Ser162=
NM_001164279.2:c.265_267delinsAGC NP_001157751.1:p.Ser89=
NM_001164280.2:c.484_486delinsAGC NP_001157752.1:p.Ser162=
NM_001467.6:c.484_486delinsAGC NP_001458.1:p.Ser162=
NM_001164277.2:c.484_486delinsAGC MANE Select NP_001157749.1:p.Ser162=