Canonical Allele Identifier: CA2259210969

Gene: PGAP3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39687871G= , CM000679.2:g.39687871G=	GRCh38
NC_000017.10:g.37844124G= , CM000679.1:g.37844124G=	GRCh37
NC_000017.9:g.35097650G=	NCBI36
NG_007503.1:g.4732G= , LRG_724:g.4732G=
NG_034125.1:g.5200C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300658.9:c.144C= MANE Select	ENSP00000300658.4:p.His48=
ENST00000300658.8:c.144C=	ENSP00000300658.4:p.His48=
ENST00000309862.10:n.187C=
ENST00000378011.8:c.144C=	ENSP00000367250.4:p.His48=
ENST00000429199.6:c.144C=	ENSP00000415765.2:p.His48=
ENST00000579146.5:c.144C=	ENSP00000463234.1:p.His48=
ENST00000582276.1:n.179C=
ENST00000584620.5:c.131C=
ENST00000584856.1:c.-35-1852C=	ENSP00000463785.1:n.-35-1852C=
ENST00000614824.4:c.144C=	ENSP00000480165.1:p.His48=
NM_001291726.1:c.144C=	NP_001278655.1:p.His48=
NM_001291728.1:c.144C=	NP_001278657.1:p.His48=
NM_001291730.1:c.144C=	NP_001278659.1:p.His48=
NM_001291732.1:c.144C=	NP_001278661.1:p.His48=
NM_001291733.1:c.144C=	NP_001278662.1:p.His48=
NM_033419.4:c.144C=	NP_219487.3:p.His48=
XM_011525480.1:c.144C=	XP_011523782.1:p.His48=
XM_011525481.1:c.-344C=	XP_011523783.1:n.-344C=
XR_934601.1:n.187C=
XM_011525480.2:c.144C=	XP_011523782.1:p.His48=
XM_011525481.2:c.-344C=	XP_011523783.1:n.-344C=
XR_002958086.1:n.187C=
NM_033419.5:c.144C= MANE Select	NP_219487.3:p.His48=
NM_001291726.2:c.144C=	NP_001278655.1:p.His48=
NM_001291728.2:c.144C=	NP_001278657.1:p.His48=
NM_001291730.2:c.144C=	NP_001278659.1:p.His48=
NM_001291732.2:c.144C=	NP_001278661.1:p.His48=
NM_001291733.2:c.144C=	NP_001278662.1:p.His48=