Canonical Allele Identifier: CA747494698

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs1307221272
• MyVariant Identifiers: chr21:g.19653051del (hg19) ; chr21:g.18280734del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18280738del , CM000683.2:g.18280738del	GRCh38
NC_000021.8:g.19653055del , CM000683.1:g.19653055del	GRCh37
NC_000021.7:g.18574926del	NCBI36
NG_012207.1:g.127920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2668+306del MANE Select	ENSP00000284885.3:n.2668+306del
ENST00000284885.7:c.2668+306del	ENSP00000284885.3:n.2668+306del
NM_002772.2:c.2668+306del	NP_002763.2:n.2668+306del
XM_011529654.1:c.2803+306del	XP_011527956.1:n.2803+306del
XM_011529655.1:c.2803+306del	XP_011527957.1:n.2803+306del
XM_011529656.1:c.2803+306del	XP_011527958.1:n.2803+306del
XM_011529657.1:c.2758+306del	XP_011527959.1:n.2758+306del
XM_011529658.1:c.2722+306del	XP_011527960.1:n.2722+306del
XM_011529659.1:c.2713+306del	XP_011527961.1:n.2713+306del
XM_011529654.2:c.2803+306del	XP_011527956.1:n.2803+306del
XM_011529656.2:c.2803+306del	XP_011527958.1:n.2803+306del
XM_011529657.2:c.2758+306del	XP_011527959.1:n.2758+306del
XM_011529658.2:c.2722+306del	XP_011527960.1:n.2722+306del
NM_002772.3:c.2668+306del MANE Select	NP_002763.3:n.2668+306del