Canonical Allele Identifier: CA2379736645

Gene: TMPRSS15

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281064G= , CM000683.2:g.18281064G=	GRCh38
NC_000021.8:g.19653381G= , CM000683.1:g.19653381G=	GRCh37
NC_000021.7:g.18575252G=	NCBI36
NG_012207.1:g.127590C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2644C= MANE Select	ENSP00000284885.3:p.Leu882=
ENST00000284885.7:c.2644C=	ENSP00000284885.3:p.Leu882=
NM_002772.2:c.2644C=	NP_002763.2:p.Leu882=
XM_011529654.1:c.2779C=	XP_011527956.1:p.Leu927=
XM_011529655.1:c.2779C=	XP_011527957.1:p.Leu927=
XM_011529656.1:c.2779C=	XP_011527958.1:p.Leu927=
XM_011529657.1:c.2734C=	XP_011527959.1:p.Leu912=
XM_011529658.1:c.2698C=	XP_011527960.1:p.Leu900=
XM_011529659.1:c.2689C=	XP_011527961.1:p.Leu897=
XM_011529654.2:c.2779C=	XP_011527956.1:p.Leu927=
XM_011529656.2:c.2779C=	XP_011527958.1:p.Leu927=
XM_011529657.2:c.2734C=	XP_011527959.1:p.Leu912=
XM_011529658.2:c.2698C=	XP_011527960.1:p.Leu900=
NM_002772.3:c.2644C= MANE Select	NP_002763.3:p.Leu882=