Canonical Allele Identifier: CA405246061

Gene: GPI

Linked Data

• dbSNP Id: rs1423498902
• gnomAD v4: 19-34399589-G-A
• MyVariant Identifiers: chr19:g.34890494G>A (hg19) ; chr19:g.34399589G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399589G>A , CM000681.2:g.34399589G>A	GRCh38
NC_000019.9:g.34890494G>A , CM000681.1:g.34890494G>A	GRCh37
NC_000019.8:g.39582334G>A	NCBI36
NG_012838.2:g.39850G>A
NG_012838.3:g.44998G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1432G>A MANE Select	ENSP00000348877.3:p.Val478Met
ENST00000415930.8:c.1549G>A	ENSP00000405573.3:p.Val517Met
ENST00000586425.2:c.1158-147G>A
ENST00000588991.7:c.1465G>A	ENSP00000465858.3:p.Val489Met
ENST00000643067.1:n.2477G>A
ENST00000647446.1:c.*483G>A	ENSP00000495129.1:n.*483G>A
ENST00000356487.9:c.1432G>A	ENSP00000348877.3:p.Val478Met
ENST00000415930.7:c.1465G>A	ENSP00000405573.2:p.Val489Met
ENST00000586077.1:n.2307G>A
ENST00000586392.1:n.1170G>A
ENST00000586425.1:c.1398+254G>A	ENSP00000467670.2:n.1398+254G>A
ENST00000588991.6:c.1477G>A	ENSP00000465858.2:p.Val493Met
ENST00000592740.5:c.193+2932G>A
NM_000175.3:c.1432G>A	NP_000166.2:p.Val478Met
NM_001184722.1:c.1465G>A	NP_001171651.1:p.Val489Met
NM_001289789.1:c.1549G>A	NP_001276718.1:p.Val517Met
NM_001289790.1:c.1348G>A	NP_001276719.1:p.Val450Met
XM_005258764.1:c.1432G>A	XP_005258821.1:p.Val478Met
XM_006723148.1:c.1432G>A	XP_006723211.1:p.Val478Met
XM_011526754.1:c.1549G>A	XP_011525056.1:p.Val517Met
NM_000175.5:c.1432G>A MANE Select	NP_000166.2:p.Val478Met
NM_001289790.2:c.1348G>A	NP_001276719.1:p.Val450Met
NM_001329909.1:c.1432G>A	NP_001316838.1:p.Val478Met
NM_001329910.1:c.1432G>A	NP_001316839.1:p.Val478Met
NM_001329911.1:c.1405G>A	NP_001316840.1:p.Val469Met
XM_011526754.3:c.1549G>A	XP_011525056.1:p.Val517Met
NM_001289790.3:c.1348G>A	NP_001276719.1:p.Val450Met
NM_001329911.2:c.1405G>A	NP_001316840.1:p.Val469Met