Canonical Allele Identifier: CA2379736801

Gene: TMPRSS15

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281420C= , CM000683.2:g.18281420C=	GRCh38
NC_000021.8:g.19653737C= , CM000683.1:g.19653737C=	GRCh37
NC_000021.7:g.18575608C=	NCBI36
NG_012207.1:g.127234G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2487-199G= MANE Select	ENSP00000284885.3:n.2487-199G=
ENST00000284885.7:c.2487-199G=	ENSP00000284885.3:n.2487-199G=
NM_002772.2:c.2487-199G=	NP_002763.2:n.2487-199G=
XM_011529654.1:c.2622-199G=	XP_011527956.1:n.2622-199G=
XM_011529655.1:c.2622-199G=	XP_011527957.1:n.2622-199G=
XM_011529656.1:c.2622-199G=	XP_011527958.1:n.2622-199G=
XM_011529657.1:c.2577-199G=	XP_011527959.1:n.2577-199G=
XM_011529658.1:c.2541-199G=	XP_011527960.1:n.2541-199G=
XM_011529659.1:c.2532-199G=	XP_011527961.1:n.2532-199G=
XM_011529654.2:c.2622-199G=	XP_011527956.1:n.2622-199G=
XM_011529656.2:c.2622-199G=	XP_011527958.1:n.2622-199G=
XM_011529657.2:c.2577-199G=	XP_011527959.1:n.2577-199G=
XM_011529658.2:c.2541-199G=	XP_011527960.1:n.2541-199G=
NM_002772.3:c.2487-199G= MANE Select	NP_002763.3:n.2487-199G=