Canonical Allele Identifier: CA409848011

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs2074693163
• gnomAD v3: 21-18281121-C-T
• gnomAD v4: 21-18281121-C-T
• MyVariant Identifiers: chr21:g.19653438C>T (hg19) ; chr21:g.18281121C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281121C>T , CM000683.2:g.18281121C>T	GRCh38
NC_000021.8:g.19653438C>T , CM000683.1:g.19653438C>T	GRCh37
NC_000021.7:g.18575309C>T	NCBI36
NG_012207.1:g.127533G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2587G>A MANE Select	ENSP00000284885.3:p.Val863Ile
ENST00000284885.7:c.2587G>A	ENSP00000284885.3:p.Val863Ile
NM_002772.2:c.2587G>A	NP_002763.2:p.Val863Ile
XM_011529654.1:c.2722G>A	XP_011527956.1:p.Val908Ile
XM_011529655.1:c.2722G>A	XP_011527957.1:p.Val908Ile
XM_011529656.1:c.2722G>A	XP_011527958.1:p.Val908Ile
XM_011529657.1:c.2677G>A	XP_011527959.1:p.Val893Ile
XM_011529658.1:c.2641G>A	XP_011527960.1:p.Val881Ile
XM_011529659.1:c.2632G>A	XP_011527961.1:p.Val878Ile
XM_011529654.2:c.2722G>A	XP_011527956.1:p.Val908Ile
XM_011529656.2:c.2722G>A	XP_011527958.1:p.Val908Ile
XM_011529657.2:c.2677G>A	XP_011527959.1:p.Val893Ile
XM_011529658.2:c.2641G>A	XP_011527960.1:p.Val881Ile
NM_002772.3:c.2587G>A MANE Select	NP_002763.3:p.Val863Ile