Canonical Allele Identifier: CA409848060

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs1302085961
• gnomAD v2: 21-19653465-T-A
• MyVariant Identifiers: chr21:g.19653465T>A (hg19) ; chr21:g.18281148T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281148T>A , CM000683.2:g.18281148T>A	GRCh38
NC_000021.8:g.19653465T>A , CM000683.1:g.19653465T>A	GRCh37
NC_000021.7:g.18575336T>A	NCBI36
NG_012207.1:g.127506A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2560A>T MANE Select	ENSP00000284885.3:p.Thr854Ser
ENST00000284885.7:c.2560A>T	ENSP00000284885.3:p.Thr854Ser
NM_002772.2:c.2560A>T	NP_002763.2:p.Thr854Ser
XM_011529654.1:c.2695A>T	XP_011527956.1:p.Thr899Ser
XM_011529655.1:c.2695A>T	XP_011527957.1:p.Thr899Ser
XM_011529656.1:c.2695A>T	XP_011527958.1:p.Thr899Ser
XM_011529657.1:c.2650A>T	XP_011527959.1:p.Thr884Ser
XM_011529658.1:c.2614A>T	XP_011527960.1:p.Thr872Ser
XM_011529659.1:c.2605A>T	XP_011527961.1:p.Thr869Ser
XM_011529654.2:c.2695A>T	XP_011527956.1:p.Thr899Ser
XM_011529656.2:c.2695A>T	XP_011527958.1:p.Thr899Ser
XM_011529657.2:c.2650A>T	XP_011527959.1:p.Thr884Ser
XM_011529658.2:c.2614A>T	XP_011527960.1:p.Thr872Ser
NM_002772.3:c.2560A>T MANE Select	NP_002763.3:p.Thr854Ser