Canonical Allele Identifier: CA2546751732

Gene: PIGP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.37065547_37065550del , CM000683.2:g.37065547_37065550del	GRCh38
NC_000021.8:g.38437847_38437850del , CM000683.1:g.38437847_38437850del	GRCh37
NC_000021.7:g.37359717_37359720del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360525.9:c.*39_*42del MANE Select	ENSP00000353719.3:n.*39_*42del
ENST00000329667.7:n.393_396del
ENST00000360525.8:c.*39_*42del	ENSP00000353719.3:n.*39_*42del
ENST00000399098.5:c.*39_*42del	ENSP00000382049.1:n.*39_*42del
ENST00000399102.5:c.*39_*42del	ENSP00000382053.1:n.*39_*42del
ENST00000399103.5:c.*39_*42del	ENSP00000382054.1:n.*39_*42del
ENST00000464265.5:c.*39_*42del	ENSP00000420037.1:n.*39_*42del
NM_153681.2:c.*39_*42del	NP_710148.1:n.*39_*42del
NM_153682.2:c.*39_*42del	NP_710149.1:n.*39_*42del
NR_028352.1:n.791_794del
XM_005260990.3:c.*39_*42del	XP_005261047.1:n.*39_*42del
XM_011529595.1:c.*39_*42del	XP_011527897.1:n.*39_*42del
XM_011529596.1:c.*39_*42del	XP_011527898.1:n.*39_*42del
NM_001320480.1:c.*39_*42del	NP_001307409.1:n.*39_*42del
NM_016430.3:c.*39_*42del	NP_057514.2:n.*39_*42del
XM_017028365.1:c.*39_*42del	XP_016883854.1:n.*39_*42del
NM_001320480.2:c.*39_*42del	NP_001307409.1:n.*39_*42del
NM_016430.4:c.*39_*42del	NP_057514.2:n.*39_*42del
NM_153682.3:c.*39_*42del MANE Select	NP_710149.1:n.*39_*42del