Canonical Allele Identifier: CA2388296209

Gene: PIGP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.37065696A= , CM000683.2:g.37065696A=	GRCh38
NC_000021.8:g.38437996A= , CM000683.1:g.38437996A=	GRCh37
NC_000021.7:g.37359866A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360525.9:c.291T= MANE Select	ENSP00000353719.3:p.Asn97=
ENST00000329667.7:n.240T=
ENST00000360525.8:c.291T=	ENSP00000353719.3:p.Asn97=
ENST00000399098.5:c.213T=	ENSP00000382049.1:p.Asn71=
ENST00000399102.5:c.291T=	ENSP00000382053.1:p.Asn97=
ENST00000399103.5:c.291T=	ENSP00000382054.1:p.Asn97=
ENST00000464265.5:c.363T=	ENSP00000420037.1:p.Asn121=
NM_153681.2:c.363T=	NP_710148.1:p.Asn121=
NM_153682.2:c.291T=	NP_710149.1:p.Asn97=
NR_028352.1:n.638T=
XM_005260990.3:c.291T=	XP_005261047.1:p.Asn97=
XM_011529595.1:c.291T=	XP_011527897.1:p.Asn97=
XM_011529596.1:c.291T=	XP_011527898.1:p.Asn97=
NM_001320480.1:c.291T=	NP_001307409.1:p.Asn97=
NM_016430.3:c.213T=	NP_057514.2:p.Asn71=
XM_017028365.1:c.213T=	XP_016883854.1:p.Asn71=
NM_001320480.2:c.291T=	NP_001307409.1:p.Asn97=
NM_016430.4:c.213T=	NP_057514.2:p.Asn71=
NM_153682.3:c.291T= MANE Select	NP_710149.1:p.Asn97=