Canonical Allele Identifier: CA2577464983

Gene: TMPRSS15

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281225_18281231dup , CM000683.2:g.18281225_18281231dup	GRCh38
NC_000021.8:g.19653542_19653548dup , CM000683.1:g.19653542_19653548dup	GRCh37
NC_000021.7:g.18575413_18575419dup	NCBI36
NG_012207.1:g.127425_127431dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2487-8_2487-2dup MANE Select	ENSP00000284885.3:n.2487-8_2487-2dup
ENST00000284885.7:c.2487-8_2487-2dup	ENSP00000284885.3:n.2487-8_2487-2dup
NM_002772.2:c.2487-8_2487-2dup	NP_002763.2:n.2487-8_2487-2dup
XM_011529654.1:c.2622-8_2622-2dup	XP_011527956.1:n.2622-8_2622-2dup
XM_011529655.1:c.2622-8_2622-2dup	XP_011527957.1:n.2622-8_2622-2dup
XM_011529656.1:c.2622-8_2622-2dup	XP_011527958.1:n.2622-8_2622-2dup
XM_011529657.1:c.2577-8_2577-2dup	XP_011527959.1:n.2577-8_2577-2dup
XM_011529658.1:c.2541-8_2541-2dup	XP_011527960.1:n.2541-8_2541-2dup
XM_011529659.1:c.2532-8_2532-2dup	XP_011527961.1:n.2532-8_2532-2dup
XM_011529654.2:c.2622-8_2622-2dup	XP_011527956.1:n.2622-8_2622-2dup
XM_011529656.2:c.2622-8_2622-2dup	XP_011527958.1:n.2622-8_2622-2dup
XM_011529657.2:c.2577-8_2577-2dup	XP_011527959.1:n.2577-8_2577-2dup
XM_011529658.2:c.2541-8_2541-2dup	XP_011527960.1:n.2541-8_2541-2dup
NM_002772.3:c.2487-8_2487-2dup MANE Select	NP_002763.3:n.2487-8_2487-2dup