Canonical Allele Identifier: CA2733567287
Gene: PGAP3 HGNC NCBI

Linked Data

dbSNP Id: rs2145165597

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39687679_39687680insAGACAGGGGCATCAGAGTGAGTGAGCTCTGGA , CM000679.2:g.39687679_39687680insAGACAGGGGCATCAGAGTGAGTGAGCTCTGGA GRCh38
NC_000017.10:g.37843932_37843933insAGACAGGGGCATCAGAGTGAGTGAGCTCTGGA , CM000679.1:g.37843932_37843933insAGACAGGGGCATCAGAGTGAGTGAGCTCTGGA GRCh37
NC_000017.9:g.35097458_35097459insAGACAGGGGCATCAGAGTGAGTGAGCTCTGGA NCBI36
NG_007503.1:g.4540_4541insAGACAGGGGCATCAGAGTGAGTGAGCTCTGGA , LRG_724:g.4540_4541insAGACAGGGGCATCAGAGTGAGTGAGCTCTGGA
NG_034125.1:g.5393_5394insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000300658.9:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC MANE Select ENSP00000300658.4:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCC...
ENST00000300658.8:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC ENSP00000300658.4:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCC...
ENST00000309862.10:n.224+156_224+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC
ENST00000378011.8:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC ENSP00000367250.4:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCC...
ENST00000429199.6:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC ENSP00000415765.2:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCC...
ENST00000579146.5:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC ENSP00000463234.1:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCC...
ENST00000582276.1:n.216+156_216+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC
ENST00000584620.5:c.168+156_168+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC
ENST00000584856.1:c.-35-1659_-35-1658insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC ENSP00000463785.1:n.-35-1659_-35-1658insCAGAGCTCACTCACTCTGATG...
ENST00000614824.4:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC ENSP00000480165.1:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCC...
NM_001291726.1:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC NP_001278655.1:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCT...
NM_001291728.1:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC NP_001278657.1:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCT...
NM_001291730.1:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC NP_001278659.1:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCT...
NM_001291732.1:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC NP_001278661.1:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCT...
NM_001291733.1:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC NP_001278662.1:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCT...
NM_033419.4:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC NP_219487.3:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTC...
XM_011525480.1:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC XP_011523782.1:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCT...
XM_011525481.1:c.-307+156_-307+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC XP_011523783.1:n.-307+156_-307+157insCAGAGCTCACTCACTCTGATGCCC...
XR_934601.1:n.224+156_224+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC
XM_011525480.2:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC XP_011523782.1:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCT...
XM_011525481.2:c.-307+156_-307+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC XP_011523783.1:n.-307+156_-307+157insCAGAGCTCACTCACTCTGATGCCC...
XR_002958086.1:n.224+156_224+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC
NM_033419.5:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC MANE Select NP_219487.3:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTC...
NM_001291726.2:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC NP_001278655.1:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCT...
NM_001291728.2:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC NP_001278657.1:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCT...
NM_001291730.2:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC NP_001278659.1:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCT...
NM_001291732.2:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC NP_001278661.1:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCT...
NM_001291733.2:c.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCTGTCTTC NP_001278662.1:n.181+156_181+157insCAGAGCTCACTCACTCTGATGCCCCT...