Canonical Allele Identifier: CA2654449990

Gene: PIGP

Linked Data

• gnomAD v4: 21-37065585-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.37065590del , CM000683.2:g.37065590del	GRCh38
NC_000021.8:g.38437890del , CM000683.1:g.38437890del	GRCh37
NC_000021.7:g.37359760del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360525.9:c.401del MANE Select	ENSP00000353719.3:p.Asn134ThrfsTer29
ENST00000329667.7:n.350del
ENST00000360525.8:c.401del	ENSP00000353719.3:p.Asn134ThrfsTer29
ENST00000399098.5:c.323del	ENSP00000382049.1:p.Asn108ThrfsTer29
ENST00000399102.5:c.401del	ENSP00000382053.1:p.Asn134ThrfsTer29
ENST00000399103.5:c.401del	ENSP00000382054.1:p.Asn134ThrfsTer29
ENST00000464265.5:c.473del	ENSP00000420037.1:p.Asn158ThrfsTer29
NM_153681.2:c.473del	NP_710148.1:p.Asn158ThrfsTer29
NM_153682.2:c.401del	NP_710149.1:p.Asn134ThrfsTer29
NR_028352.1:n.748del
XM_005260990.3:c.401del	XP_005261047.1:p.Asn134ThrfsTer29
XM_011529595.1:c.401del	XP_011527897.1:p.Asn134ThrfsTer29
XM_011529596.1:c.401del	XP_011527898.1:p.Asn134ThrfsTer29
NM_001320480.1:c.401del	NP_001307409.1:p.Asn134ThrfsTer29
NM_016430.3:c.323del	NP_057514.2:p.Asn108ThrfsTer29
XM_017028365.1:c.323del	XP_016883854.1:p.Asn108ThrfsTer29
NM_001320480.2:c.401del	NP_001307409.1:p.Asn134ThrfsTer29
NM_016430.4:c.323del	NP_057514.2:p.Asn108ThrfsTer29
NM_153682.3:c.401del MANE Select	NP_710149.1:p.Asn134ThrfsTer29