Canonical Allele Identifier: CA881701897

Gene: GPI

Linked Data

• dbSNP Id: rs1357897186
• gnomAD v3: 19-34400087-C-A
• gnomAD v4: 19-34400087-C-A
• MyVariant Identifiers: chr19:g.34890992C>A (hg19) ; chr19:g.34400087C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34400087C>A , CM000681.2:g.34400087C>A	GRCh38
NC_000019.9:g.34890992C>A , CM000681.1:g.34890992C>A	GRCh37
NC_000019.8:g.39582832C>A	NCBI36
NG_012838.2:g.40348C>A
NG_012838.3:g.45496C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.*51C>A MANE Select	ENSP00000348877.3:n.*51C>A
ENST00000415930.8:c.*51C>A	ENSP00000405573.3:n.*51C>A
ENST00000586425.2:c.1394C>A
ENST00000588991.7:c.*51C>A	ENSP00000465858.3:n.*51C>A
ENST00000643067.1:n.2773C>A
ENST00000647446.1:c.*779C>A	ENSP00000495129.1:n.*779C>A
ENST00000356487.9:c.*51C>A	ENSP00000348877.3:n.*51C>A
ENST00000415930.7:c.*51C>A	ENSP00000405573.2:n.*51C>A
ENST00000586077.1:n.2805C>A
ENST00000586392.1:n.1466C>A
ENST00000586425.1:c.*160C>A	ENSP00000467670.2:n.*160C>A
ENST00000588991.6:c.1773C>A	ENSP00000465858.2:n.1773C>A
ENST00000592740.5:c.193+3430C>A
NM_000175.3:c.*51C>A	NP_000166.2:n.*51C>A
NM_001184722.1:c.*51C>A	NP_001171651.1:n.*51C>A
NM_001289789.1:c.*51C>A	NP_001276718.1:n.*51C>A
NM_001289790.1:c.*51C>A	NP_001276719.1:n.*51C>A
XM_005258764.1:c.*51C>A	XP_005258821.1:n.*51C>A
XM_006723148.1:c.*51C>A	XP_006723211.1:n.*51C>A
XM_011526754.1:c.*51C>A	XP_011525056.1:n.*51C>A
NM_000175.5:c.*51C>A MANE Select	NP_000166.2:n.*51C>A
NM_001289790.2:c.*51C>A	NP_001276719.1:n.*51C>A
NM_001329909.1:c.*51C>A	NP_001316838.1:n.*51C>A
NM_001329910.1:c.*51C>A	NP_001316839.1:n.*51C>A
NM_001329911.1:c.*51C>A	NP_001316840.1:n.*51C>A
XM_011526754.3:c.*51C>A	XP_011525056.1:n.*51C>A
NM_001289790.3:c.*51C>A	NP_001276719.1:n.*51C>A
NM_001329911.2:c.*51C>A	NP_001316840.1:n.*51C>A