Canonical Allele Identifier: CA2637630955
Gene: PGAP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39671980_39671983del , CM000679.2:g.39671980_39671983del GRCh38
NC_000017.10:g.37828233_37828236del , CM000679.1:g.37828233_37828236del GRCh37
NC_000017.9:g.35081759_35081762del NCBI36
NG_034125.1:g.21093_21096del
NG_042278.1:g.9000_9003del

Transcript Alleles

HGVS Amino-acid Change
ENST00000300658.9:c.*825_*828del MANE Select ENSP00000300658.4:n.*825_*828del
ENST00000300658.8:c.*825_*828del ENSP00000300658.4:n.*825_*828del
ENST00000309862.10:n.2173_2176del
ENST00000378011.8:c.*825_*828del ENSP00000367250.4:n.*825_*828del
ENST00000579146.5:c.*874_*877del ENSP00000463234.1:n.*874_*877del
ENST00000614824.4:c.*825_*828del ENSP00000480165.1:n.*825_*828del
ENST00000619169.4:c.714_717del ENSP00000478028.1:p.Trp238CysfsTer6
NM_001291726.1:c.*825_*828del NP_001278655.1:n.*825_*828del
NM_001291728.1:c.*825_*828del NP_001278657.1:n.*825_*828del
NM_001291730.1:c.*825_*828del NP_001278659.1:n.*825_*828del
NM_001291732.1:c.*825_*828del NP_001278661.1:n.*825_*828del
NM_001291733.1:c.*874_*877del NP_001278662.1:n.*874_*877del
NM_033419.4:c.*825_*828del NP_219487.3:n.*825_*828del
XM_011525480.2:c.*857_*860del XP_011523782.1:n.*857_*860del
XM_011525481.2:c.*825_*828del XP_011523783.1:n.*825_*828del
XR_002958086.1:n.2315_2318del
NM_033419.5:c.*825_*828del MANE Select NP_219487.3:n.*825_*828del
NM_001291726.2:c.*825_*828del NP_001278655.1:n.*825_*828del
NM_001291728.2:c.*825_*828del NP_001278657.1:n.*825_*828del
NM_001291730.2:c.*825_*828del NP_001278659.1:n.*825_*828del
NM_001291732.2:c.*825_*828del NP_001278661.1:n.*825_*828del
NM_001291733.2:c.*874_*877del NP_001278662.1:n.*874_*877del