Canonical Allele Identifier: CA2388296231
Gene: PIGP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.37065733_37065735delinsGCT , CM000683.2:g.37065733_37065735delinsGCT GRCh38
NC_000021.8:g.38438033_38438035delinsGCT , CM000683.1:g.38438033_38438035delinsGCT GRCh37
NC_000021.7:g.37359903_37359905delinsGCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360525.9:c.275-23_275-21delinsAGC MANE Select ENSP00000353719.3:n.275-23_275-21delinsAGC
ENST00000329667.7:n.224-23_224-21delinsAGC
ENST00000360525.8:c.275-23_275-21delinsAGC ENSP00000353719.3:n.275-23_275-21delinsAGC
ENST00000399098.5:c.197-23_197-21delinsAGC ENSP00000382049.1:n.197-23_197-21delinsAGC
ENST00000399102.5:c.275-23_275-21delinsAGC ENSP00000382053.1:n.275-23_275-21delinsAGC
ENST00000399103.5:c.275-23_275-21delinsAGC ENSP00000382054.1:n.275-23_275-21delinsAGC
ENST00000464265.5:c.347-23_347-21delinsAGC ENSP00000420037.1:n.347-23_347-21delinsAGC
NM_153681.2:c.347-23_347-21delinsAGC NP_710148.1:n.347-23_347-21delinsAGC
NM_153682.2:c.275-23_275-21delinsAGC NP_710149.1:n.275-23_275-21delinsAGC
NR_028352.1:n.622-23_622-21delinsAGC
XM_005260990.3:c.275-23_275-21delinsAGC XP_005261047.1:n.275-23_275-21delinsAGC
XM_011529595.1:c.275-23_275-21delinsAGC XP_011527897.1:n.275-23_275-21delinsAGC
XM_011529596.1:c.275-23_275-21delinsAGC XP_011527898.1:n.275-23_275-21delinsAGC
NM_001320480.1:c.275-23_275-21delinsAGC NP_001307409.1:n.275-23_275-21delinsAGC
NM_016430.3:c.197-23_197-21delinsAGC NP_057514.2:n.197-23_197-21delinsAGC
XM_017028365.1:c.197-23_197-21delinsAGC XP_016883854.1:n.197-23_197-21delinsAGC
NM_001320480.2:c.275-23_275-21delinsAGC NP_001307409.1:n.275-23_275-21delinsAGC
NM_016430.4:c.197-23_197-21delinsAGC NP_057514.2:n.197-23_197-21delinsAGC
NM_153682.3:c.275-23_275-21delinsAGC MANE Select NP_710149.1:n.275-23_275-21delinsAGC