Canonical Allele Identifier: CA318130246

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs994512837
• MyVariant Identifiers: chr21:g.19653467T>G (hg19) ; chr21:g.18281150T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281150T>G , CM000683.2:g.18281150T>G	GRCh38
NC_000021.8:g.19653467T>G , CM000683.1:g.19653467T>G	GRCh37
NC_000021.7:g.18575338T>G	NCBI36
NG_012207.1:g.127504A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2558A>C MANE Select	ENSP00000284885.3:p.Gln853Pro
ENST00000284885.7:c.2558A>C	ENSP00000284885.3:p.Gln853Pro
NM_002772.2:c.2558A>C	NP_002763.2:p.Gln853Pro
XM_011529654.1:c.2693A>C	XP_011527956.1:p.Gln898Pro
XM_011529655.1:c.2693A>C	XP_011527957.1:p.Gln898Pro
XM_011529656.1:c.2693A>C	XP_011527958.1:p.Gln898Pro
XM_011529657.1:c.2648A>C	XP_011527959.1:p.Gln883Pro
XM_011529658.1:c.2612A>C	XP_011527960.1:p.Gln871Pro
XM_011529659.1:c.2603A>C	XP_011527961.1:p.Gln868Pro
XM_011529654.2:c.2693A>C	XP_011527956.1:p.Gln898Pro
XM_011529656.2:c.2693A>C	XP_011527958.1:p.Gln898Pro
XM_011529657.2:c.2648A>C	XP_011527959.1:p.Gln883Pro
XM_011529658.2:c.2612A>C	XP_011527960.1:p.Gln871Pro
NM_002772.3:c.2558A>C MANE Select	NP_002763.3:p.Gln853Pro