Canonical Allele Identifier: CA2577464982

Gene: TMPRSS15

Linked Data

• gnomAD v4: 21-18281212-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281213_18281214del , CM000683.2:g.18281213_18281214del	GRCh38
NC_000021.8:g.19653530_19653531del , CM000683.1:g.19653530_19653531del	GRCh37
NC_000021.7:g.18575401_18575402del	NCBI36
NG_012207.1:g.127440_127441del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2494_2495del MANE Select	ENSP00000284885.3:p.Leu832ArgfsTer29
ENST00000284885.7:c.2494_2495del	ENSP00000284885.3:p.Leu832ArgfsTer29
NM_002772.2:c.2494_2495del	NP_002763.2:p.Leu832ArgfsTer29
XM_011529654.1:c.2629_2630del	XP_011527956.1:p.Leu877ArgfsTer29
XM_011529655.1:c.2629_2630del	XP_011527957.1:p.Leu877ArgfsTer29
XM_011529656.1:c.2629_2630del	XP_011527958.1:p.Leu877ArgfsTer29
XM_011529657.1:c.2584_2585del	XP_011527959.1:p.Leu862ArgfsTer29
XM_011529658.1:c.2548_2549del	XP_011527960.1:p.Leu850ArgfsTer29
XM_011529659.1:c.2539_2540del	XP_011527961.1:p.Leu847ArgfsTer29
XM_011529654.2:c.2629_2630del	XP_011527956.1:p.Leu877ArgfsTer29
XM_011529656.2:c.2629_2630del	XP_011527958.1:p.Leu877ArgfsTer29
XM_011529657.2:c.2584_2585del	XP_011527959.1:p.Leu862ArgfsTer29
XM_011529658.2:c.2548_2549del	XP_011527960.1:p.Leu850ArgfsTer29
NM_002772.3:c.2494_2495del MANE Select	NP_002763.3:p.Leu832ArgfsTer29