Canonical Allele Identifier: CA645581667
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027726_119027727delinsAA , CM000673.2:g.119027726_119027727delinsAA GRCh38
NC_000011.9:g.118898436_118898437delinsAA , CM000673.1:g.118898436_118898437delinsAA GRCh37
NC_000011.8:g.118403646_118403647delinsAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.756_757delinsTT
ENST00000697845.1:n.680_681delinsTT
ENST00000697846.1:n.756_757delinsTT
ENST00000697847.1:n.756_757delinsTT
ENST00000697848.1:n.756_757delinsTT
ENST00000697849.1:n.1795_1796delinsTT
ENST00000697850.1:n.756_757delinsTT
ENST00000697851.1:n.2116_2117delinsTT
ENST00000638186.1:n.830_831delinsTT
ENST00000638360.1:n.662_663delinsTT
ENST00000638925.1:n.763_764delinsTT
ENST00000650539.1:n.932_933delinsTT
ENST00000330775.9:c.527_528delinsTT ENSP00000476242.2:p.Trp176Phe
ENST00000357590.9:c.527_528delinsTT ENSP00000476176.2:p.Trp176Phe
ENST00000524428.5:n.848_849delinsTT
ENST00000525039.5:n.950_951delinsTT
ENST00000525102.5:n.1284_1285delinsTT
ENST00000525372.5:n.527_528delinsTT
ENST00000526275.5:n.1308_1309delinsTT
ENST00000526626.6:n.489_490delinsTT
ENST00000527992.5:n.754_755delinsTT
ENST00000529510.5:n.399+467_399+468delinsTT
ENST00000530407.5:n.676_677delinsTT
ENST00000532085.1:n.3137_3138delinsTT
ENST00000532888.6:n.822_823delinsTT
ENST00000538950.5:c.308_309delinsTT ENSP00000475991.2:p.Trp103Phe
ENST00000545985.5:c.527_528delinsTT ENSP00000475241.2:p.Trp176Phe