Canonical Allele Identifier: CA363058659

Gene: TRIM15

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30171922G>C , CM000668.2:g.30171922G>C	GRCh38
NC_000006.11:g.30139699G>C , CM000668.1:g.30139699G>C	GRCh37
NC_000006.10:g.30247678G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_033229.3:c.971G>C MANE Select	NP_150232.2:p.Ser324Thr
ENST00000376694.9:c.971G>C MANE Select	ENSP00000365884.4:p.Ser324Thr
NM_033229.2:c.971G>C	NP_150232.2:p.Ser324Thr
ENST00000376688.2:c.305-642G>C	ENSP00000365878.2:n.305-642G>C
ENST00000376694.8:c.971G>C	ENSP00000365884.4:p.Ser324Thr
ENST00000433744.1:c.458G>C
ENST00000619857.4:c.764G>C	ENSP00000484001.1:p.Ser255Thr
XM_011514987.1:c.656G>C	XP_011513289.1:p.Ser219Thr
XM_011514988.1:c.350G>C	XP_011513290.1:p.Ser117Thr
XM_011514988.2:c.350G>C	XP_011513290.1:p.Ser117Thr