Canonical Allele Identifier: CA2379736531

Gene: TMPRSS15

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18280789G= , CM000683.2:g.18280789G=	GRCh38
NC_000021.8:g.19653106G= , CM000683.1:g.19653106G=	GRCh37
NC_000021.7:g.18574977G=	NCBI36
NG_012207.1:g.127865C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2668+251C= MANE Select	ENSP00000284885.3:n.2668+251C=
ENST00000284885.7:c.2668+251C=	ENSP00000284885.3:n.2668+251C=
NM_002772.2:c.2668+251C=	NP_002763.2:n.2668+251C=
XM_011529654.1:c.2803+251C=	XP_011527956.1:n.2803+251C=
XM_011529655.1:c.2803+251C=	XP_011527957.1:n.2803+251C=
XM_011529656.1:c.2803+251C=	XP_011527958.1:n.2803+251C=
XM_011529657.1:c.2758+251C=	XP_011527959.1:n.2758+251C=
XM_011529658.1:c.2722+251C=	XP_011527960.1:n.2722+251C=
XM_011529659.1:c.2713+251C=	XP_011527961.1:n.2713+251C=
XM_011529654.2:c.2803+251C=	XP_011527956.1:n.2803+251C=
XM_011529656.2:c.2803+251C=	XP_011527958.1:n.2803+251C=
XM_011529657.2:c.2758+251C=	XP_011527959.1:n.2758+251C=
XM_011529658.2:c.2722+251C=	XP_011527960.1:n.2722+251C=
NM_002772.3:c.2668+251C= MANE Select	NP_002763.3:n.2668+251C=