Canonical Allele Identifier: CA409918146

Gene: PIGP

Linked Data

• MyVariant Identifiers: chr21:g.38437917A>T (hg19) ; chr21:g.37065617A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.37065617A>T , CM000683.2:g.37065617A>T	GRCh38
NC_000021.8:g.38437917A>T , CM000683.1:g.38437917A>T	GRCh37
NC_000021.7:g.37359787A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360525.9:c.370T>A MANE Select	ENSP00000353719.3:p.Phe124Ile
ENST00000329667.7:n.319T>A
ENST00000360525.8:c.370T>A	ENSP00000353719.3:p.Phe124Ile
ENST00000399098.5:c.292T>A	ENSP00000382049.1:p.Phe98Ile
ENST00000399102.5:c.370T>A	ENSP00000382053.1:p.Phe124Ile
ENST00000399103.5:c.370T>A	ENSP00000382054.1:p.Phe124Ile
ENST00000464265.5:c.442T>A	ENSP00000420037.1:p.Phe148Ile
NM_153681.2:c.442T>A	NP_710148.1:p.Phe148Ile
NM_153682.2:c.370T>A	NP_710149.1:p.Phe124Ile
NR_028352.1:n.717T>A
XM_005260990.3:c.370T>A	XP_005261047.1:p.Phe124Ile
XM_011529595.1:c.370T>A	XP_011527897.1:p.Phe124Ile
XM_011529596.1:c.370T>A	XP_011527898.1:p.Phe124Ile
NM_001320480.1:c.370T>A	NP_001307409.1:p.Phe124Ile
NM_016430.3:c.292T>A	NP_057514.2:p.Phe98Ile
XM_017028365.1:c.292T>A	XP_016883854.1:p.Phe98Ile
NM_001320480.2:c.370T>A	NP_001307409.1:p.Phe124Ile
NM_016430.4:c.292T>A	NP_057514.2:p.Phe98Ile
NM_153682.3:c.370T>A MANE Select	NP_710149.1:p.Phe124Ile