Canonical Allele Identifier: CA2654083098

Gene: TMPRSS15

Linked Data

• gnomAD v4: 21-18281211-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281212dup , CM000683.2:g.18281212dup	GRCh38
NC_000021.8:g.19653529dup , CM000683.1:g.19653529dup	GRCh37
NC_000021.7:g.18575400dup	NCBI36
NG_012207.1:g.127442dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2496dup MANE Select	ENSP00000284885.3:p.Glu833ArgfsTer29
ENST00000284885.7:c.2496dup	ENSP00000284885.3:p.Glu833ArgfsTer29
NM_002772.2:c.2496dup	NP_002763.2:p.Glu833ArgfsTer29
XM_011529654.1:c.2631dup	XP_011527956.1:p.Glu878ArgfsTer29
XM_011529655.1:c.2631dup	XP_011527957.1:p.Glu878ArgfsTer29
XM_011529656.1:c.2631dup	XP_011527958.1:p.Glu878ArgfsTer29
XM_011529657.1:c.2586dup	XP_011527959.1:p.Glu863ArgfsTer29
XM_011529658.1:c.2550dup	XP_011527960.1:p.Glu851ArgfsTer29
XM_011529659.1:c.2541dup	XP_011527961.1:p.Glu848ArgfsTer29
XM_011529654.2:c.2631dup	XP_011527956.1:p.Glu878ArgfsTer29
XM_011529656.2:c.2631dup	XP_011527958.1:p.Glu878ArgfsTer29
XM_011529657.2:c.2586dup	XP_011527959.1:p.Glu863ArgfsTer29
XM_011529658.2:c.2550dup	XP_011527960.1:p.Glu851ArgfsTer29
NM_002772.3:c.2496dup MANE Select	NP_002763.3:p.Glu833ArgfsTer29