Canonical Allele Identifier: CA2259203983

Gene: PGAP3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39672032T= , CM000679.2:g.39672032T=	GRCh38
NC_000017.10:g.37828285T= , CM000679.1:g.37828285T=	GRCh37
NC_000017.9:g.35081811T=	NCBI36
NG_034125.1:g.21039A=
NG_042278.1:g.9052T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300658.9:c.*771A= MANE Select	ENSP00000300658.4:n.*771A=
ENST00000300658.8:c.*771A=	ENSP00000300658.4:n.*771A=
ENST00000309862.10:n.2119A=
ENST00000378011.8:c.*771A=	ENSP00000367250.4:n.*771A=
ENST00000579146.5:c.*820A=	ENSP00000463234.1:n.*820A=
ENST00000614824.4:c.*771A=	ENSP00000480165.1:n.*771A=
ENST00000619169.4:c.660A=	ENSP00000478028.1:p.Arg220=
NM_001291726.1:c.*771A=	NP_001278655.1:n.*771A=
NM_001291728.1:c.*771A=	NP_001278657.1:n.*771A=
NM_001291730.1:c.*771A=	NP_001278659.1:n.*771A=
NM_001291732.1:c.*771A=	NP_001278661.1:n.*771A=
NM_001291733.1:c.*820A=	NP_001278662.1:n.*820A=
NM_033419.4:c.*771A=	NP_219487.3:n.*771A=
XM_011525480.2:c.*803A=	XP_011523782.1:n.*803A=
XM_011525481.2:c.*771A=	XP_011523783.1:n.*771A=
XR_002958086.1:n.2261A=
NM_033419.5:c.*771A= MANE Select	NP_219487.3:n.*771A=
NM_001291726.2:c.*771A=	NP_001278655.1:n.*771A=
NM_001291728.2:c.*771A=	NP_001278657.1:n.*771A=
NM_001291730.2:c.*771A=	NP_001278659.1:n.*771A=
NM_001291732.2:c.*771A=	NP_001278661.1:n.*771A=
NM_001291733.2:c.*820A=	NP_001278662.1:n.*820A=