Canonical Allele Identifier: CA658799406

Gene: TMPRSS15

Linked Data

• ClinVar Variation Id: 523101
• ClinVar RCV Id: RCV000626320
• dbSNP Id: rs1555909961
• MyVariant Identifiers: chr21:g.19770637_19770641del (hg19) ; chr21:g.18398320_18398324del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18398320_18398324del , CM000683.2:g.18398320_18398324del	GRCh38
NC_000021.8:g.19770637_19770641del , CM000683.1:g.19770637_19770641del	GRCh37
NC_000021.7:g.18692508_18692512del	NCBI36
NG_012207.1:g.10330_10334del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.151_155del MANE Select	ENSP00000284885.3:p.Ala51TrpfsTer5
ENST00000284885.7:c.151_155del	ENSP00000284885.3:p.Ala51TrpfsTer5
ENST00000422787.1:c.16_20del	ENSP00000398253.1:p.Ala6TrpfsTer5
ENST00000474775.1:c.-277-14546_-277-14542del	ENSP00000474811.1:n.-277-14546_-277-14542del
NM_002772.2:c.151_155del	NP_002763.2:p.Ala51TrpfsTer5
XM_011529654.1:c.151_155del	XP_011527956.1:p.Ala51TrpfsTer5
XM_011529655.1:c.151_155del	XP_011527957.1:p.Ala51TrpfsTer5
XM_011529656.1:c.151_155del	XP_011527958.1:p.Ala51TrpfsTer5
XM_011529657.1:c.151_155del	XP_011527959.1:p.Ala51TrpfsTer5
XM_011529658.1:c.151_155del	XP_011527960.1:p.Ala51TrpfsTer5
XM_011529659.1:c.151_155del	XP_011527961.1:p.Ala51TrpfsTer5
XM_011529654.2:c.151_155del	XP_011527956.1:p.Ala51TrpfsTer5
XM_011529656.2:c.151_155del	XP_011527958.1:p.Ala51TrpfsTer5
XM_011529657.2:c.151_155del	XP_011527959.1:p.Ala51TrpfsTer5
XM_011529658.2:c.151_155del	XP_011527960.1:p.Ala51TrpfsTer5
NM_002772.3:c.151_155del MANE Select	NP_002763.3:p.Ala51TrpfsTer5