Canonical Allele Identifier: CA399315399
Gene: PGAP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39672150A>T , CM000679.2:g.39672150A>T GRCh38
NC_000017.10:g.37828403A>T , CM000679.1:g.37828403A>T GRCh37
NC_000017.9:g.35081929A>T NCBI36
NG_034125.1:g.20921T>A
NG_042278.1:g.9170A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300658.9:c.*653T>A MANE Select ENSP00000300658.4:n.*653T>A
ENST00000300658.8:c.*653T>A ENSP00000300658.4:n.*653T>A
ENST00000309862.10:n.2001T>A
ENST00000378011.8:c.*653T>A ENSP00000367250.4:n.*653T>A
ENST00000579146.5:c.*702T>A ENSP00000463234.1:n.*702T>A
ENST00000614824.4:c.*653T>A ENSP00000480165.1:n.*653T>A
ENST00000619169.4:c.542T>A ENSP00000478028.1:p.Leu181Gln
NM_001291726.1:c.*653T>A NP_001278655.1:n.*653T>A
NM_001291728.1:c.*653T>A NP_001278657.1:n.*653T>A
NM_001291730.1:c.*653T>A NP_001278659.1:n.*653T>A
NM_001291732.1:c.*653T>A NP_001278661.1:n.*653T>A
NM_001291733.1:c.*702T>A NP_001278662.1:n.*702T>A
NM_033419.4:c.*653T>A NP_219487.3:n.*653T>A
XM_011525481.1:c.*653T>A XP_011523783.1:n.*653T>A
XM_011525480.2:c.*685T>A XP_011523782.1:n.*685T>A
XM_011525481.2:c.*653T>A XP_011523783.1:n.*653T>A
XR_002958086.1:n.2143T>A
NM_033419.5:c.*653T>A MANE Select NP_219487.3:n.*653T>A
NM_001291726.2:c.*653T>A NP_001278655.1:n.*653T>A
NM_001291728.2:c.*653T>A NP_001278657.1:n.*653T>A
NM_001291730.2:c.*653T>A NP_001278659.1:n.*653T>A
NM_001291732.2:c.*653T>A NP_001278661.1:n.*653T>A
NM_001291733.2:c.*702T>A NP_001278662.1:n.*702T>A