Canonical Allele Identifier: CA405246571

Gene: GPI

Linked Data

• MyVariant Identifiers: chr19:g.34890811A>G (hg19) ; chr19:g.34399906A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399906A>G , CM000681.2:g.34399906A>G	GRCh38
NC_000019.9:g.34890811A>G , CM000681.1:g.34890811A>G	GRCh37
NC_000019.8:g.39582651A>G	NCBI36
NG_012838.2:g.40167A>G
NG_012838.3:g.45315A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356487.11:c.1547A>G MANE Select	ENSP00000348877.3:p.Glu516Gly
ENST00000415930.8:c.1664A>G	ENSP00000405573.3:p.Glu555Gly
ENST00000586425.2:c.1213A>G
ENST00000588991.7:c.1580A>G	ENSP00000465858.3:p.Glu527Gly
ENST00000643067.1:n.2592A>G
ENST00000647446.1:c.*598A>G	ENSP00000495129.1:n.*598A>G
ENST00000356487.9:c.1547A>G	ENSP00000348877.3:p.Glu516Gly
ENST00000415930.7:c.1580A>G	ENSP00000405573.2:p.Glu527Gly
ENST00000586077.1:n.2624A>G
ENST00000586392.1:n.1285A>G
ENST00000586425.1:c.1404A>G	ENSP00000467670.2:p.Gly468=
ENST00000588991.6:c.1592A>G	ENSP00000465858.2:p.Glu531Gly
ENST00000592740.5:c.193+3249A>G
NM_000175.3:c.1547A>G	NP_000166.2:p.Glu516Gly
NM_001184722.1:c.1580A>G	NP_001171651.1:p.Glu527Gly
NM_001289789.1:c.1664A>G	NP_001276718.1:p.Glu555Gly
NM_001289790.1:c.1463A>G	NP_001276719.1:p.Glu488Gly
XM_005258764.1:c.1547A>G	XP_005258821.1:p.Glu516Gly
XM_006723148.1:c.1547A>G	XP_006723211.1:p.Glu516Gly
XM_011526754.1:c.1664A>G	XP_011525056.1:p.Glu555Gly
NM_000175.5:c.1547A>G MANE Select	NP_000166.2:p.Glu516Gly
NM_001289790.2:c.1463A>G	NP_001276719.1:p.Glu488Gly
NM_001329909.1:c.1547A>G	NP_001316838.1:p.Glu516Gly
NM_001329910.1:c.1547A>G	NP_001316839.1:p.Glu516Gly
NM_001329911.1:c.1520A>G	NP_001316840.1:p.Glu507Gly
XM_011526754.3:c.1664A>G	XP_011525056.1:p.Glu555Gly
NM_001289790.3:c.1463A>G	NP_001276719.1:p.Glu488Gly
NM_001329911.2:c.1520A>G	NP_001316840.1:p.Glu507Gly