Canonical Allele Identifier: CA2379736634
Gene: TMPRSS15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.18281040_18281044delinsCTGTG , CM000683.2:g.18281040_18281044delinsCTGTG GRCh38
NC_000021.8:g.19653357_19653361delinsCTGTG , CM000683.1:g.19653357_19653361delinsCTGTG GRCh37
NC_000021.7:g.18575228_18575232delinsCTGTG NCBI36
NG_012207.1:g.127610_127614delinsCACAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000284885.8:c.2664_2668delinsCACAG MANE Select ENSP00000284885.3:p.Tyr888=
ENST00000284885.7:c.2664_2668delinsCACAG ENSP00000284885.3:p.Tyr888=
NM_002772.2:c.2664_2668delinsCACAG NP_002763.2:p.Tyr888=
XM_011529654.1:c.2799_2803delinsCACAG XP_011527956.1:p.Tyr933=
XM_011529655.1:c.2799_2803delinsCACAG XP_011527957.1:p.Tyr933=
XM_011529656.1:c.2799_2803delinsCACAG XP_011527958.1:p.Tyr933=
XM_011529657.1:c.2754_2758delinsCACAG XP_011527959.1:p.Tyr918=
XM_011529658.1:c.2718_2722delinsCACAG XP_011527960.1:p.Tyr906=
XM_011529659.1:c.2709_2713delinsCACAG XP_011527961.1:p.Tyr903=
XM_011529654.2:c.2799_2803delinsCACAG XP_011527956.1:p.Tyr933=
XM_011529656.2:c.2799_2803delinsCACAG XP_011527958.1:p.Tyr933=
XM_011529657.2:c.2754_2758delinsCACAG XP_011527959.1:p.Tyr918=
XM_011529658.2:c.2718_2722delinsCACAG XP_011527960.1:p.Tyr906=
NM_002772.3:c.2664_2668delinsCACAG MANE Select NP_002763.3:p.Tyr888=