Canonical Allele Identifier: CA2259204216

Gene: PGAP3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39672329A= , CM000679.2:g.39672329A=	GRCh38
NC_000017.10:g.37828582A= , CM000679.1:g.37828582A=	GRCh37
NC_000017.9:g.35082108A=	NCBI36
NG_034125.1:g.20742T=
NG_042278.1:g.9349A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300658.9:c.*474T= MANE Select	ENSP00000300658.4:n.*474T=
ENST00000300658.8:c.*474T=	ENSP00000300658.4:n.*474T=
ENST00000309862.10:n.1822T=
ENST00000378011.8:c.*474T=	ENSP00000367250.4:n.*474T=
ENST00000579146.5:c.*523T=	ENSP00000463234.1:n.*523T=
ENST00000614824.4:c.*474T=	ENSP00000480165.1:n.*474T=
ENST00000619169.4:c.363T=	ENSP00000478028.1:p.Leu121=
NM_001291726.1:c.*474T=	NP_001278655.1:n.*474T=
NM_001291728.1:c.*474T=	NP_001278657.1:n.*474T=
NM_001291730.1:c.*474T=	NP_001278659.1:n.*474T=
NM_001291732.1:c.*474T=	NP_001278661.1:n.*474T=
NM_001291733.1:c.*523T=	NP_001278662.1:n.*523T=
NM_033419.4:c.*474T=	NP_219487.3:n.*474T=
XM_011525481.1:c.*474T=	XP_011523783.1:n.*474T=
XM_011525480.2:c.*506T=	XP_011523782.1:n.*506T=
XM_011525481.2:c.*474T=	XP_011523783.1:n.*474T=
XR_002958086.1:n.1964T=
NM_033419.5:c.*474T= MANE Select	NP_219487.3:n.*474T=
NM_001291726.2:c.*474T=	NP_001278655.1:n.*474T=
NM_001291728.2:c.*474T=	NP_001278657.1:n.*474T=
NM_001291730.2:c.*474T=	NP_001278659.1:n.*474T=
NM_001291732.2:c.*474T=	NP_001278661.1:n.*474T=
NM_001291733.2:c.*523T=	NP_001278662.1:n.*523T=