Canonical Allele Identifier: CA409848056

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs1344057441
• gnomAD v3: 21-18281145-C-T
• gnomAD v4: 21-18281145-C-T
• MyVariant Identifiers: chr21:g.19653462C>T (hg19) ; chr21:g.18281145C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281145C>T , CM000683.2:g.18281145C>T	GRCh38
NC_000021.8:g.19653462C>T , CM000683.1:g.19653462C>T	GRCh37
NC_000021.7:g.18575333C>T	NCBI36
NG_012207.1:g.127509G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2563G>A MANE Select	ENSP00000284885.3:p.Val855Ile
ENST00000284885.7:c.2563G>A	ENSP00000284885.3:p.Val855Ile
NM_002772.2:c.2563G>A	NP_002763.2:p.Val855Ile
XM_011529654.1:c.2698G>A	XP_011527956.1:p.Val900Ile
XM_011529655.1:c.2698G>A	XP_011527957.1:p.Val900Ile
XM_011529656.1:c.2698G>A	XP_011527958.1:p.Val900Ile
XM_011529657.1:c.2653G>A	XP_011527959.1:p.Val885Ile
XM_011529658.1:c.2617G>A	XP_011527960.1:p.Val873Ile
XM_011529659.1:c.2608G>A	XP_011527961.1:p.Val870Ile
XM_011529654.2:c.2698G>A	XP_011527956.1:p.Val900Ile
XM_011529656.2:c.2698G>A	XP_011527958.1:p.Val900Ile
XM_011529657.2:c.2653G>A	XP_011527959.1:p.Val885Ile
XM_011529658.2:c.2617G>A	XP_011527960.1:p.Val873Ile
NM_002772.3:c.2563G>A MANE Select	NP_002763.3:p.Val855Ile