Canonical Allele Identifier: CA409848057

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs1402595546
• gnomAD v2: 21-19653464-G-A
• gnomAD v4: 21-18281147-G-A
• MyVariant Identifiers: chr21:g.19653464G>A (hg19) ; chr21:g.18281147G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2561C>T MANE Select	ENSP00000284885.3:p.Thr854Ile
ENST00000284885.7:c.2561C>T	ENSP00000284885.3:p.Thr854Ile
NM_002772.2:c.2561C>T	NP_002763.2:p.Thr854Ile
XM_011529654.1:c.2696C>T	XP_011527956.1:p.Thr899Ile
XM_011529655.1:c.2696C>T	XP_011527957.1:p.Thr899Ile
XM_011529656.1:c.2696C>T	XP_011527958.1:p.Thr899Ile
XM_011529657.1:c.2651C>T	XP_011527959.1:p.Thr884Ile
XM_011529658.1:c.2615C>T	XP_011527960.1:p.Thr872Ile
XM_011529659.1:c.2606C>T	XP_011527961.1:p.Thr869Ile
XM_011529654.2:c.2696C>T	XP_011527956.1:p.Thr899Ile
XM_011529656.2:c.2696C>T	XP_011527958.1:p.Thr899Ile
XM_011529657.2:c.2651C>T	XP_011527959.1:p.Thr884Ile
XM_011529658.2:c.2615C>T	XP_011527960.1:p.Thr872Ile
NM_002772.3:c.2561C>T MANE Select	NP_002763.3:p.Thr854Ile