Canonical Allele Identifier: CA2388296208

Gene: PIGP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.37065696_37065697delinsAT , CM000683.2:g.37065696_37065697delinsAT	GRCh38
NC_000021.8:g.38437996_38437997delinsAT , CM000683.1:g.38437996_38437997delinsAT	GRCh37
NC_000021.7:g.37359866_37359867delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360525.9:c.290_291delinsAT MANE Select	ENSP00000353719.3:p.Asn97=
ENST00000329667.7:n.239_240delinsAT
ENST00000360525.8:c.290_291delinsAT	ENSP00000353719.3:p.Asn97=
ENST00000399098.5:c.212_213delinsAT	ENSP00000382049.1:p.Asn71=
ENST00000399102.5:c.290_291delinsAT	ENSP00000382053.1:p.Asn97=
ENST00000399103.5:c.290_291delinsAT	ENSP00000382054.1:p.Asn97=
ENST00000464265.5:c.362_363delinsAT	ENSP00000420037.1:p.Asn121=
NM_153681.2:c.362_363delinsAT	NP_710148.1:p.Asn121=
NM_153682.2:c.290_291delinsAT	NP_710149.1:p.Asn97=
NR_028352.1:n.637_638delinsAT
XM_005260990.3:c.290_291delinsAT	XP_005261047.1:p.Asn97=
XM_011529595.1:c.290_291delinsAT	XP_011527897.1:p.Asn97=
XM_011529596.1:c.290_291delinsAT	XP_011527898.1:p.Asn97=
NM_001320480.1:c.290_291delinsAT	NP_001307409.1:p.Asn97=
NM_016430.3:c.212_213delinsAT	NP_057514.2:p.Asn71=
XM_017028365.1:c.212_213delinsAT	XP_016883854.1:p.Asn71=
NM_001320480.2:c.290_291delinsAT	NP_001307409.1:p.Asn97=
NM_016430.4:c.212_213delinsAT	NP_057514.2:p.Asn71=
NM_153682.3:c.290_291delinsAT MANE Select	NP_710149.1:p.Asn97=