Canonical Allele Identifier: CA409848074

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653471G>T (hg19) ; chr21:g.18281154G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281154G>T , CM000683.2:g.18281154G>T	GRCh38
NC_000021.8:g.19653471G>T , CM000683.1:g.19653471G>T	GRCh37
NC_000021.7:g.18575342G>T	NCBI36
NG_012207.1:g.127500C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2554C>A MANE Select	ENSP00000284885.3:p.Pro852Thr
ENST00000284885.7:c.2554C>A	ENSP00000284885.3:p.Pro852Thr
NM_002772.2:c.2554C>A	NP_002763.2:p.Pro852Thr
XM_011529654.1:c.2689C>A	XP_011527956.1:p.Pro897Thr
XM_011529655.1:c.2689C>A	XP_011527957.1:p.Pro897Thr
XM_011529656.1:c.2689C>A	XP_011527958.1:p.Pro897Thr
XM_011529657.1:c.2644C>A	XP_011527959.1:p.Pro882Thr
XM_011529658.1:c.2608C>A	XP_011527960.1:p.Pro870Thr
XM_011529659.1:c.2599C>A	XP_011527961.1:p.Pro867Thr
XM_011529654.2:c.2689C>A	XP_011527956.1:p.Pro897Thr
XM_011529656.2:c.2689C>A	XP_011527958.1:p.Pro897Thr
XM_011529657.2:c.2644C>A	XP_011527959.1:p.Pro882Thr
XM_011529658.2:c.2608C>A	XP_011527960.1:p.Pro870Thr
NM_002772.3:c.2554C>A MANE Select	NP_002763.3:p.Pro852Thr