Canonical Allele Identifier: CA409918122
Gene: PIGP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.37065613A>T , CM000683.2:g.37065613A>T GRCh38
NC_000021.8:g.38437913A>T , CM000683.1:g.38437913A>T GRCh37
NC_000021.7:g.37359783A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360525.9:c.374T>A MANE Select ENSP00000353719.3:p.Leu125His
ENST00000329667.7:n.323T>A
ENST00000360525.8:c.374T>A ENSP00000353719.3:p.Leu125His
ENST00000399098.5:c.296T>A ENSP00000382049.1:p.Leu99His
ENST00000399102.5:c.374T>A ENSP00000382053.1:p.Leu125His
ENST00000399103.5:c.374T>A ENSP00000382054.1:p.Leu125His
ENST00000464265.5:c.446T>A ENSP00000420037.1:p.Leu149His
NM_153681.2:c.446T>A NP_710148.1:p.Leu149His
NM_153682.2:c.374T>A NP_710149.1:p.Leu125His
NR_028352.1:n.721T>A
XM_005260990.3:c.374T>A XP_005261047.1:p.Leu125His
XM_011529595.1:c.374T>A XP_011527897.1:p.Leu125His
XM_011529596.1:c.374T>A XP_011527898.1:p.Leu125His
NM_001320480.1:c.374T>A NP_001307409.1:p.Leu125His
NM_016430.3:c.296T>A NP_057514.2:p.Leu99His
XM_017028365.1:c.296T>A XP_016883854.1:p.Leu99His
NM_001320480.2:c.374T>A NP_001307409.1:p.Leu125His
NM_016430.4:c.296T>A NP_057514.2:p.Leu99His
NM_153682.3:c.374T>A MANE Select NP_710149.1:p.Leu125His