Canonical Allele Identifier: CA409848008

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs1446358035
• gnomAD v2: 21-19653437-A-T
• COSMIC: COSM6446746
• MyVariant Identifiers: chr21:g.19653437A>T (hg19) ; chr21:g.18281120A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281120A>T , CM000683.2:g.18281120A>T	GRCh38
NC_000021.8:g.19653437A>T , CM000683.1:g.19653437A>T	GRCh37
NC_000021.7:g.18575308A>T	NCBI36
NG_012207.1:g.127534T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2588T>A MANE Select	ENSP00000284885.3:p.Val863Asp
ENST00000284885.7:c.2588T>A	ENSP00000284885.3:p.Val863Asp
NM_002772.2:c.2588T>A	NP_002763.2:p.Val863Asp
XM_011529654.1:c.2723T>A	XP_011527956.1:p.Val908Asp
XM_011529655.1:c.2723T>A	XP_011527957.1:p.Val908Asp
XM_011529656.1:c.2723T>A	XP_011527958.1:p.Val908Asp
XM_011529657.1:c.2678T>A	XP_011527959.1:p.Val893Asp
XM_011529658.1:c.2642T>A	XP_011527960.1:p.Val881Asp
XM_011529659.1:c.2633T>A	XP_011527961.1:p.Val878Asp
XM_011529654.2:c.2723T>A	XP_011527956.1:p.Val908Asp
XM_011529656.2:c.2723T>A	XP_011527958.1:p.Val908Asp
XM_011529657.2:c.2678T>A	XP_011527959.1:p.Val893Asp
XM_011529658.2:c.2642T>A	XP_011527960.1:p.Val881Asp
NM_002772.3:c.2588T>A MANE Select	NP_002763.3:p.Val863Asp