Canonical Allele Identifier: CA409847851

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs2074691666
• gnomAD v4: 21-18281052-C-T
• MyVariant Identifiers: chr21:g.19653369C>T (hg19) ; chr21:g.18281052C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281052C>T , CM000683.2:g.18281052C>T	GRCh38
NC_000021.8:g.19653369C>T , CM000683.1:g.19653369C>T	GRCh37
NC_000021.7:g.18575240C>T	NCBI36
NG_012207.1:g.127602G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2656G>A MANE Select	ENSP00000284885.3:p.Val886Met
ENST00000284885.7:c.2656G>A	ENSP00000284885.3:p.Val886Met
NM_002772.2:c.2656G>A	NP_002763.2:p.Val886Met
XM_011529654.1:c.2791G>A	XP_011527956.1:p.Val931Met
XM_011529655.1:c.2791G>A	XP_011527957.1:p.Val931Met
XM_011529656.1:c.2791G>A	XP_011527958.1:p.Val931Met
XM_011529657.1:c.2746G>A	XP_011527959.1:p.Val916Met
XM_011529658.1:c.2710G>A	XP_011527960.1:p.Val904Met
XM_011529659.1:c.2701G>A	XP_011527961.1:p.Val901Met
XM_011529654.2:c.2791G>A	XP_011527956.1:p.Val931Met
XM_011529656.2:c.2791G>A	XP_011527958.1:p.Val931Met
XM_011529657.2:c.2746G>A	XP_011527959.1:p.Val916Met
XM_011529658.2:c.2710G>A	XP_011527960.1:p.Val904Met
NM_002772.3:c.2656G>A MANE Select	NP_002763.3:p.Val886Met