Canonical Allele Identifier: CA2259203932

Gene: PGAP3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39671911G= , CM000679.2:g.39671911G=	GRCh38
NC_000017.10:g.37828164G= , CM000679.1:g.37828164G=	GRCh37
NC_000017.9:g.35081690G=	NCBI36
NG_034125.1:g.21160C=
NG_042278.1:g.8931G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300658.9:c.*892C= MANE Select	ENSP00000300658.4:n.*892C=
ENST00000300658.8:c.*892C=	ENSP00000300658.4:n.*892C=
ENST00000309862.10:n.2240C=
ENST00000378011.8:c.*892C=	ENSP00000367250.4:n.*892C=
ENST00000579146.5:c.*941C=	ENSP00000463234.1:n.*941C=
ENST00000614824.4:c.*892C=	ENSP00000480165.1:n.*892C=
ENST00000619169.4:c.*58C=	ENSP00000478028.1:n.*58C=
NM_001291726.1:c.*892C=	NP_001278655.1:n.*892C=
NM_001291728.1:c.*892C=	NP_001278657.1:n.*892C=
NM_001291730.1:c.*892C=	NP_001278659.1:n.*892C=
NM_001291732.1:c.*892C=	NP_001278661.1:n.*892C=
NM_001291733.1:c.*941C=	NP_001278662.1:n.*941C=
NM_033419.4:c.*892C=	NP_219487.3:n.*892C=
XM_011525480.2:c.*924C=	XP_011523782.1:n.*924C=
XM_011525481.2:c.*892C=	XP_011523783.1:n.*892C=
XR_002958086.1:n.2382C=
NM_033419.5:c.*892C= MANE Select	NP_219487.3:n.*892C=
NM_001291726.2:c.*892C=	NP_001278655.1:n.*892C=
NM_001291728.2:c.*892C=	NP_001278657.1:n.*892C=
NM_001291730.2:c.*892C=	NP_001278659.1:n.*892C=
NM_001291732.2:c.*892C=	NP_001278661.1:n.*892C=
NM_001291733.2:c.*941C=	NP_001278662.1:n.*941C=