Canonical Allele Identifier: CA2388296207

Gene: PIGP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.37065695G= , CM000683.2:g.37065695G=	GRCh38
NC_000021.8:g.38437995G= , CM000683.1:g.38437995G=	GRCh37
NC_000021.7:g.37359865G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360525.9:c.292C= MANE Select	ENSP00000353719.3:p.Gln98=
ENST00000329667.7:n.241C=
ENST00000360525.8:c.292C=	ENSP00000353719.3:p.Gln98=
ENST00000399098.5:c.214C=	ENSP00000382049.1:p.Gln72=
ENST00000399102.5:c.292C=	ENSP00000382053.1:p.Gln98=
ENST00000399103.5:c.292C=	ENSP00000382054.1:p.Gln98=
ENST00000464265.5:c.364C=	ENSP00000420037.1:p.Gln122=
NM_153681.2:c.364C=	NP_710148.1:p.Gln122=
NM_153682.2:c.292C=	NP_710149.1:p.Gln98=
NR_028352.1:n.639C=
XM_005260990.3:c.292C=	XP_005261047.1:p.Gln98=
XM_011529595.1:c.292C=	XP_011527897.1:p.Gln98=
XM_011529596.1:c.292C=	XP_011527898.1:p.Gln98=
NM_001320480.1:c.292C=	NP_001307409.1:p.Gln98=
NM_016430.3:c.214C=	NP_057514.2:p.Gln72=
XM_017028365.1:c.214C=	XP_016883854.1:p.Gln72=
NM_001320480.2:c.292C=	NP_001307409.1:p.Gln98=
NM_016430.4:c.214C=	NP_057514.2:p.Gln72=
NM_153682.3:c.292C= MANE Select	NP_710149.1:p.Gln98=