Canonical Allele Identifier: CA637791397

Gene: PIGP

Linked Data

• dbSNP Id: rs1196789439
• gnomAD v2: 21-38437866-T-C
• gnomAD v4: 21-37065566-T-C
• MyVariant Identifiers: chr21:g.38437866T>C (hg19) ; chr21:g.37065566T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.37065566T>C , CM000683.2:g.37065566T>C	GRCh38
NC_000021.8:g.38437866T>C , CM000683.1:g.38437866T>C	GRCh37
NC_000021.7:g.37359736T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360525.9:c.*16A>G MANE Select	ENSP00000353719.3:n.*16A>G
ENST00000329667.7:n.370A>G
ENST00000360525.8:c.*16A>G	ENSP00000353719.3:n.*16A>G
ENST00000399098.5:c.*16A>G	ENSP00000382049.1:n.*16A>G
ENST00000399102.5:c.*16A>G	ENSP00000382053.1:n.*16A>G
ENST00000399103.5:c.*16A>G	ENSP00000382054.1:n.*16A>G
ENST00000464265.5:c.*16A>G	ENSP00000420037.1:n.*16A>G
NM_153681.2:c.*16A>G	NP_710148.1:n.*16A>G
NM_153682.2:c.*16A>G	NP_710149.1:n.*16A>G
NR_028352.1:n.768A>G
XM_005260990.3:c.*16A>G	XP_005261047.1:n.*16A>G
XM_011529595.1:c.*16A>G	XP_011527897.1:n.*16A>G
XM_011529596.1:c.*16A>G	XP_011527898.1:n.*16A>G
NM_001320480.1:c.*16A>G	NP_001307409.1:n.*16A>G
NM_016430.3:c.*16A>G	NP_057514.2:n.*16A>G
XM_017028365.1:c.*16A>G	XP_016883854.1:n.*16A>G
NM_001320480.2:c.*16A>G	NP_001307409.1:n.*16A>G
NM_016430.4:c.*16A>G	NP_057514.2:n.*16A>G
NM_153682.3:c.*16A>G MANE Select	NP_710149.1:n.*16A>G