Canonical Allele Identifier: CA409918311
Gene: PIGP HGNC NCBI

Linked Data

dbSNP Id: rs369586193

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.37065644A>G , CM000683.2:g.37065644A>G GRCh38
NC_000021.8:g.38437944A>G , CM000683.1:g.38437944A>G GRCh37
NC_000021.7:g.37359814A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360525.9:c.343T>C MANE Select ENSP00000353719.3:p.Ser115Pro
ENST00000329667.7:n.292T>C
ENST00000360525.8:c.343T>C ENSP00000353719.3:p.Ser115Pro
ENST00000399098.5:c.265T>C ENSP00000382049.1:p.Ser89Pro
ENST00000399102.5:c.343T>C ENSP00000382053.1:p.Ser115Pro
ENST00000399103.5:c.343T>C ENSP00000382054.1:p.Ser115Pro
ENST00000464265.5:c.415T>C ENSP00000420037.1:p.Ser139Pro
NM_153681.2:c.415T>C NP_710148.1:p.Ser139Pro
NM_153682.2:c.343T>C NP_710149.1:p.Ser115Pro
NR_028352.1:n.690T>C
XM_005260990.3:c.343T>C XP_005261047.1:p.Ser115Pro
XM_011529595.1:c.343T>C XP_011527897.1:p.Ser115Pro
XM_011529596.1:c.343T>C XP_011527898.1:p.Ser115Pro
NM_001320480.1:c.343T>C NP_001307409.1:p.Ser115Pro
NM_016430.3:c.265T>C NP_057514.2:p.Ser89Pro
XM_017028365.1:c.265T>C XP_016883854.1:p.Ser89Pro
NM_001320480.2:c.343T>C NP_001307409.1:p.Ser115Pro
NM_016430.4:c.265T>C NP_057514.2:p.Ser89Pro
NM_153682.3:c.343T>C MANE Select NP_710149.1:p.Ser115Pro