Canonical Allele Identifier: CA2388296195

Gene: PIGP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.37065660T= , CM000683.2:g.37065660T=	GRCh38
NC_000021.8:g.38437960T= , CM000683.1:g.38437960T=	GRCh37
NC_000021.7:g.37359830T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360525.9:c.327A= MANE Select	ENSP00000353719.3:p.Pro109=
ENST00000329667.7:n.276A=
ENST00000360525.8:c.327A=	ENSP00000353719.3:p.Pro109=
ENST00000399098.5:c.249A=	ENSP00000382049.1:p.Pro83=
ENST00000399102.5:c.327A=	ENSP00000382053.1:p.Pro109=
ENST00000399103.5:c.327A=	ENSP00000382054.1:p.Pro109=
ENST00000464265.5:c.399A=	ENSP00000420037.1:p.Pro133=
NM_153681.2:c.399A=	NP_710148.1:p.Pro133=
NM_153682.2:c.327A=	NP_710149.1:p.Pro109=
NR_028352.1:n.674A=
XM_005260990.3:c.327A=	XP_005261047.1:p.Pro109=
XM_011529595.1:c.327A=	XP_011527897.1:p.Pro109=
XM_011529596.1:c.327A=	XP_011527898.1:p.Pro109=
NM_001320480.1:c.327A=	NP_001307409.1:p.Pro109=
NM_016430.3:c.249A=	NP_057514.2:p.Pro83=
XM_017028365.1:c.249A=	XP_016883854.1:p.Pro83=
NM_001320480.2:c.327A=	NP_001307409.1:p.Pro109=
NM_016430.4:c.249A=	NP_057514.2:p.Pro83=
NM_153682.3:c.327A= MANE Select	NP_710149.1:p.Pro109=