Canonical Allele Identifier: CA409848186

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs2074694794
• gnomAD v4: 21-18281208-G-A
• MyVariant Identifiers: chr21:g.19653525G>A (hg19) ; chr21:g.18281208G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281208G>A , CM000683.2:g.18281208G>A	GRCh38
NC_000021.8:g.19653525G>A , CM000683.1:g.19653525G>A	GRCh37
NC_000021.7:g.18575396G>A	NCBI36
NG_012207.1:g.127446C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2500C>T MANE Select	ENSP00000284885.3:p.Pro834Ser
ENST00000284885.7:c.2500C>T	ENSP00000284885.3:p.Pro834Ser
NM_002772.2:c.2500C>T	NP_002763.2:p.Pro834Ser
XM_011529654.1:c.2635C>T	XP_011527956.1:p.Pro879Ser
XM_011529655.1:c.2635C>T	XP_011527957.1:p.Pro879Ser
XM_011529656.1:c.2635C>T	XP_011527958.1:p.Pro879Ser
XM_011529657.1:c.2590C>T	XP_011527959.1:p.Pro864Ser
XM_011529658.1:c.2554C>T	XP_011527960.1:p.Pro852Ser
XM_011529659.1:c.2545C>T	XP_011527961.1:p.Pro849Ser
XM_011529654.2:c.2635C>T	XP_011527956.1:p.Pro879Ser
XM_011529656.2:c.2635C>T	XP_011527958.1:p.Pro879Ser
XM_011529657.2:c.2590C>T	XP_011527959.1:p.Pro864Ser
XM_011529658.2:c.2554C>T	XP_011527960.1:p.Pro852Ser
NM_002772.3:c.2500C>T MANE Select	NP_002763.3:p.Pro834Ser