Canonical Allele Identifier: CA2379736512

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs2074688672

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18280751_18280754del , CM000683.2:g.18280751_18280754del	GRCh38
NC_000021.8:g.19653068_19653071del , CM000683.1:g.19653068_19653071del	GRCh37
NC_000021.7:g.18574939_18574942del	NCBI36
NG_012207.1:g.127904_127907del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2668+290_2668+293del MANE Select	ENSP00000284885.3:n.2668+290_2668+293del
ENST00000284885.7:c.2668+290_2668+293del	ENSP00000284885.3:n.2668+290_2668+293del
NM_002772.2:c.2668+290_2668+293del	NP_002763.2:n.2668+290_2668+293del
XM_011529654.1:c.2803+290_2803+293del	XP_011527956.1:n.2803+290_2803+293del
XM_011529655.1:c.2803+290_2803+293del	XP_011527957.1:n.2803+290_2803+293del
XM_011529656.1:c.2803+290_2803+293del	XP_011527958.1:n.2803+290_2803+293del
XM_011529657.1:c.2758+290_2758+293del	XP_011527959.1:n.2758+290_2758+293del
XM_011529658.1:c.2722+290_2722+293del	XP_011527960.1:n.2722+290_2722+293del
XM_011529659.1:c.2713+290_2713+293del	XP_011527961.1:n.2713+290_2713+293del
XM_011529654.2:c.2803+290_2803+293del	XP_011527956.1:n.2803+290_2803+293del
XM_011529656.2:c.2803+290_2803+293del	XP_011527958.1:n.2803+290_2803+293del
XM_011529657.2:c.2758+290_2758+293del	XP_011527959.1:n.2758+290_2758+293del
XM_011529658.2:c.2722+290_2722+293del	XP_011527960.1:n.2722+290_2722+293del
NM_002772.3:c.2668+290_2668+293del MANE Select	NP_002763.3:n.2668+290_2668+293del