Canonical Allele Identifier: CA511459142

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653463T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281146T>C , CM000683.2:g.18281146T>C	GRCh38
NC_000021.8:g.19653463T>C , CM000683.1:g.19653463T>C	GRCh37
NC_000021.7:g.18575334T>C	NCBI36
NG_012207.1:g.127508A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2562A>G MANE Select	ENSP00000284885.3:p.Thr854=
ENST00000284885.7:c.2562A>G	ENSP00000284885.3:p.Thr854=
NM_002772.2:c.2562A>G	NP_002763.2:p.Thr854=
XM_011529654.1:c.2697A>G	XP_011527956.1:p.Thr899=
XM_011529655.1:c.2697A>G	XP_011527957.1:p.Thr899=
XM_011529656.1:c.2697A>G	XP_011527958.1:p.Thr899=
XM_011529657.1:c.2652A>G	XP_011527959.1:p.Thr884=
XM_011529658.1:c.2616A>G	XP_011527960.1:p.Thr872=
XM_011529659.1:c.2607A>G	XP_011527961.1:p.Thr869=
XM_011529654.2:c.2697A>G	XP_011527956.1:p.Thr899=
XM_011529656.2:c.2697A>G	XP_011527958.1:p.Thr899=
XM_011529657.2:c.2652A>G	XP_011527959.1:p.Thr884=
XM_011529658.2:c.2616A>G	XP_011527960.1:p.Thr872=
NM_002772.3:c.2562A>G MANE Select	NP_002763.3:p.Thr854=