Canonical Allele Identifier: CA2504899186
Gene: PIGP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.37065478T>C , CM000683.2:g.37065478T>C GRCh38
NC_000021.8:g.38437778T>C , CM000683.1:g.38437778T>C GRCh37
NC_000021.7:g.37359648T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360525.9:c.*104A>G MANE Select ENSP00000353719.3:n.*104A>G
ENST00000329667.7:n.458A>G
ENST00000360525.8:c.*104A>G ENSP00000353719.3:n.*104A>G
ENST00000399098.5:c.*104A>G ENSP00000382049.1:n.*104A>G
ENST00000399102.5:c.*104A>G ENSP00000382053.1:n.*104A>G
ENST00000399103.5:c.*104A>G ENSP00000382054.1:n.*104A>G
ENST00000464265.5:c.*104A>G ENSP00000420037.1:n.*104A>G
NM_153681.2:c.*104A>G NP_710148.1:n.*104A>G
NM_153682.2:c.*104A>G NP_710149.1:n.*104A>G
NR_028352.1:n.856A>G
XM_005260990.3:c.*104A>G XP_005261047.1:n.*104A>G
XM_011529595.1:c.*104A>G XP_011527897.1:n.*104A>G
XM_011529596.1:c.*104A>G XP_011527898.1:n.*104A>G
NM_001320480.1:c.*104A>G NP_001307409.1:n.*104A>G
NM_016430.3:c.*104A>G NP_057514.2:n.*104A>G
XM_017028365.1:c.*104A>G XP_016883854.1:n.*104A>G
NM_001320480.2:c.*104A>G NP_001307409.1:n.*104A>G
NM_016430.4:c.*104A>G NP_057514.2:n.*104A>G
NM_153682.3:c.*104A>G MANE Select NP_710149.1:n.*104A>G