Canonical Allele Identifier: CA512083120

Gene: PIGP

Linked Data

• dbSNP Id: rs1601120356
• MyVariant Identifiers: chr21:g.38437891G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.37065591G>A , CM000683.2:g.37065591G>A	GRCh38
NC_000021.8:g.38437891G>A , CM000683.1:g.38437891G>A	GRCh37
NC_000021.7:g.37359761G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360525.9:c.396C>T MANE Select	ENSP00000353719.3:p.Thr132=
ENST00000329667.7:n.345C>T
ENST00000360525.8:c.396C>T	ENSP00000353719.3:p.Thr132=
ENST00000399098.5:c.318C>T	ENSP00000382049.1:p.Thr106=
ENST00000399102.5:c.396C>T	ENSP00000382053.1:p.Thr132=
ENST00000399103.5:c.396C>T	ENSP00000382054.1:p.Thr132=
ENST00000464265.5:c.468C>T	ENSP00000420037.1:p.Thr156=
NM_153681.2:c.468C>T	NP_710148.1:p.Thr156=
NM_153682.2:c.396C>T	NP_710149.1:p.Thr132=
NR_028352.1:n.743C>T
XM_005260990.3:c.396C>T	XP_005261047.1:p.Thr132=
XM_011529595.1:c.396C>T	XP_011527897.1:p.Thr132=
XM_011529596.1:c.396C>T	XP_011527898.1:p.Thr132=
NM_001320480.1:c.396C>T	NP_001307409.1:p.Thr132=
NM_016430.3:c.318C>T	NP_057514.2:p.Thr106=
XM_017028365.1:c.318C>T	XP_016883854.1:p.Thr106=
NM_001320480.2:c.396C>T	NP_001307409.1:p.Thr132=
NM_016430.4:c.318C>T	NP_057514.2:p.Thr106=
NM_153682.3:c.396C>T MANE Select	NP_710149.1:p.Thr132=