Canonical Allele Identifier: CA409848058

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653464G>C (hg19) ; chr21:g.18281147G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281147G>C , CM000683.2:g.18281147G>C	GRCh38
NC_000021.8:g.19653464G>C , CM000683.1:g.19653464G>C	GRCh37
NC_000021.7:g.18575335G>C	NCBI36
NG_012207.1:g.127507C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2561C>G MANE Select	ENSP00000284885.3:p.Thr854Arg
ENST00000284885.7:c.2561C>G	ENSP00000284885.3:p.Thr854Arg
NM_002772.2:c.2561C>G	NP_002763.2:p.Thr854Arg
XM_011529654.1:c.2696C>G	XP_011527956.1:p.Thr899Arg
XM_011529655.1:c.2696C>G	XP_011527957.1:p.Thr899Arg
XM_011529656.1:c.2696C>G	XP_011527958.1:p.Thr899Arg
XM_011529657.1:c.2651C>G	XP_011527959.1:p.Thr884Arg
XM_011529658.1:c.2615C>G	XP_011527960.1:p.Thr872Arg
XM_011529659.1:c.2606C>G	XP_011527961.1:p.Thr869Arg
XM_011529654.2:c.2696C>G	XP_011527956.1:p.Thr899Arg
XM_011529656.2:c.2696C>G	XP_011527958.1:p.Thr899Arg
XM_011529657.2:c.2651C>G	XP_011527959.1:p.Thr884Arg
XM_011529658.2:c.2615C>G	XP_011527960.1:p.Thr872Arg
NM_002772.3:c.2561C>G MANE Select	NP_002763.3:p.Thr854Arg