Canonical Allele Identifier: CA2259204166
Gene: PGAP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39672265C= , CM000679.2:g.39672265C= GRCh38
NC_000017.10:g.37828518C= , CM000679.1:g.37828518C= GRCh37
NC_000017.9:g.35082044C= NCBI36
NG_034125.1:g.20806G=
NG_042278.1:g.9285C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300658.9:c.*538G= MANE Select ENSP00000300658.4:n.*538G=
ENST00000300658.8:c.*538G= ENSP00000300658.4:n.*538G=
ENST00000309862.10:n.1886G=
ENST00000378011.8:c.*538G= ENSP00000367250.4:n.*538G=
ENST00000579146.5:c.*587G= ENSP00000463234.1:n.*587G=
ENST00000614824.4:c.*538G= ENSP00000480165.1:n.*538G=
ENST00000619169.4:c.427G= ENSP00000478028.1:p.Gly143=
NM_001291726.1:c.*538G= NP_001278655.1:n.*538G=
NM_001291728.1:c.*538G= NP_001278657.1:n.*538G=
NM_001291730.1:c.*538G= NP_001278659.1:n.*538G=
NM_001291732.1:c.*538G= NP_001278661.1:n.*538G=
NM_001291733.1:c.*587G= NP_001278662.1:n.*587G=
NM_033419.4:c.*538G= NP_219487.3:n.*538G=
XM_011525481.1:c.*538G= XP_011523783.1:n.*538G=
XM_011525480.2:c.*570G= XP_011523782.1:n.*570G=
XM_011525481.2:c.*538G= XP_011523783.1:n.*538G=
XR_002958086.1:n.2028G=
NM_033419.5:c.*538G= MANE Select NP_219487.3:n.*538G=
NM_001291726.2:c.*538G= NP_001278655.1:n.*538G=
NM_001291728.2:c.*538G= NP_001278657.1:n.*538G=
NM_001291730.2:c.*538G= NP_001278659.1:n.*538G=
NM_001291732.2:c.*538G= NP_001278661.1:n.*538G=
NM_001291733.2:c.*587G= NP_001278662.1:n.*587G=