Canonical Allele Identifier: CA409847919

Gene: TMPRSS15

Linked Data

• gnomAD v4: 21-18281081-T-C
• MyVariant Identifiers: chr21:g.19653398T>C (hg19) ; chr21:g.18281081T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281081T>C , CM000683.2:g.18281081T>C	GRCh38
NC_000021.8:g.19653398T>C , CM000683.1:g.19653398T>C	GRCh37
NC_000021.7:g.18575269T>C	NCBI36
NG_012207.1:g.127573A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2627A>G MANE Select	ENSP00000284885.3:p.Asp876Gly
ENST00000284885.7:c.2627A>G	ENSP00000284885.3:p.Asp876Gly
NM_002772.2:c.2627A>G	NP_002763.2:p.Asp876Gly
XM_011529654.1:c.2762A>G	XP_011527956.1:p.Asp921Gly
XM_011529655.1:c.2762A>G	XP_011527957.1:p.Asp921Gly
XM_011529656.1:c.2762A>G	XP_011527958.1:p.Asp921Gly
XM_011529657.1:c.2717A>G	XP_011527959.1:p.Asp906Gly
XM_011529658.1:c.2681A>G	XP_011527960.1:p.Asp894Gly
XM_011529659.1:c.2672A>G	XP_011527961.1:p.Asp891Gly
XM_011529654.2:c.2762A>G	XP_011527956.1:p.Asp921Gly
XM_011529656.2:c.2762A>G	XP_011527958.1:p.Asp921Gly
XM_011529657.2:c.2717A>G	XP_011527959.1:p.Asp906Gly
XM_011529658.2:c.2681A>G	XP_011527960.1:p.Asp894Gly
NM_002772.3:c.2627A>G MANE Select	NP_002763.3:p.Asp876Gly