Canonical Allele Identifier: CA918979936

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1555191280

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027726_119027727del , CM000673.2:g.119027726_119027727del	GRCh38
NC_000011.9:g.118898436_118898437del , CM000673.1:g.118898436_118898437del	GRCh37
NC_000011.8:g.118403646_118403647del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.756_757del
ENST00000697845.1:n.680_681del
ENST00000697846.1:n.756_757del
ENST00000697847.1:n.756_757del
ENST00000697848.1:n.756_757del
ENST00000697849.1:n.1795_1796del
ENST00000697850.1:n.756_757del
ENST00000697851.1:n.2116_2117del
ENST00000638186.1:n.830_831del
ENST00000638360.1:n.662_663del
ENST00000638925.1:n.763_764del
ENST00000650539.1:n.932_933del
ENST00000330775.9:c.527_528del	ENSP00000476242.2:p.Trp176CysfsTer14
ENST00000357590.9:c.527_528del	ENSP00000476176.2:p.Trp176CysfsTer14
ENST00000524428.5:n.848_849del
ENST00000525039.5:n.950_951del
ENST00000525102.5:n.1284_1285del
ENST00000525372.5:n.527_528del
ENST00000526275.5:n.1308_1309del
ENST00000526626.6:n.489_490del
ENST00000527992.5:n.754_755del
ENST00000529510.5:n.399+467_399+468del
ENST00000530407.5:n.676_677del
ENST00000532085.1:n.3137_3138del
ENST00000532888.6:n.822_823del
ENST00000538950.5:c.308_309del	ENSP00000475991.2:p.Trp103CysfsTer14
ENST00000545985.5:c.527_528del	ENSP00000475241.2:p.Trp176CysfsTer14