Canonical Allele Identifier: CA3047141957

Gene: TRIM15

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30171922_30171923delinsAT , CM000668.2:g.30171922_30171923delinsAT	GRCh38
NC_000006.11:g.30139699_30139700delinsAT , CM000668.1:g.30139699_30139700delinsAT	GRCh37
NC_000006.10:g.30247678_30247679delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_033229.3:c.971_972delinsAT MANE Select	NP_150232.2:p.Ser324Asn
ENST00000376694.9:c.971_972delinsAT MANE Select	ENSP00000365884.4:p.Ser324Asn
NM_033229.2:c.971_972delinsAT	NP_150232.2:p.Ser324Asn
ENST00000376688.2:c.305-642_305-641delinsAT	ENSP00000365878.2:n.305-642_305-641delinsAT
ENST00000376694.8:c.971_972delinsAT	ENSP00000365884.4:p.Ser324Asn
ENST00000433744.1:c.458_459delinsAT
ENST00000619857.4:c.764_765delinsAT	ENSP00000484001.1:p.Ser255Asn
XM_011514987.1:c.656_657delinsAT	XP_011513289.1:p.Ser219Asn
XM_011514988.1:c.350_351delinsAT	XP_011513290.1:p.Ser117Asn
XM_011514988.2:c.350_351delinsAT	XP_011513290.1:p.Ser117Asn