Canonical Allele Identifier: CA2379773825

Gene: TMPRSS15

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18359856G= , CM000683.2:g.18359856G=	GRCh38
NC_000021.8:g.19732173G= , CM000683.1:g.19732173G=	GRCh37
NC_000021.7:g.18654044G=	NCBI36
NG_012207.1:g.48798C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002772.3:c.781C= MANE Select	NP_002763.3:p.Gln261=
ENST00000284885.8:c.781C= MANE Select	ENSP00000284885.3:p.Gln261=
NM_002772.2:c.781C=	NP_002763.2:p.Gln261=
ENST00000284885.7:c.781C=	ENSP00000284885.3:p.Gln261=
XM_011529654.1:c.916C=	XP_011527956.1:p.Gln306=
XM_011529654.2:c.916C=	XP_011527956.1:p.Gln306=
XM_011529655.1:c.916C=	XP_011527957.1:p.Gln306=
XM_011529656.1:c.916C=	XP_011527958.1:p.Gln306=
XM_011529656.2:c.916C=	XP_011527958.1:p.Gln306=
XM_011529657.1:c.871C=	XP_011527959.1:p.Gln291=
XM_011529657.2:c.871C=	XP_011527959.1:p.Gln291=
XM_011529658.1:c.835C=	XP_011527960.1:p.Gln279=
XM_011529658.2:c.835C=	XP_011527960.1:p.Gln279=
XM_011529659.1:c.826C=	XP_011527961.1:p.Gln276=