Canonical Allele Identifier: CA307634424

Gene: GPI

Linked Data

• dbSNP Id: rs372480304
• gnomAD v2: 19-34890633-A-G
• gnomAD v4: 19-34399728-A-G
• MyVariant Identifiers: chr19:g.34890633A>G (hg19) ; chr19:g.34399728A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399728A>G , CM000681.2:g.34399728A>G	GRCh38
NC_000019.9:g.34890633A>G , CM000681.1:g.34890633A>G	GRCh37
NC_000019.8:g.39582473A>G	NCBI36
NG_012838.2:g.39989A>G
NG_012838.3:g.45137A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1484A>G MANE Select	ENSP00000348877.3:p.Glu495Gly
ENST00000415930.8:c.1601A>G	ENSP00000405573.3:p.Glu534Gly
ENST00000586425.2:c.1158-8A>G
ENST00000588991.7:c.1517A>G	ENSP00000465858.3:p.Glu506Gly
ENST00000643067.1:n.2529A>G
ENST00000647446.1:c.*535A>G	ENSP00000495129.1:n.*535A>G
ENST00000356487.9:c.1484A>G	ENSP00000348877.3:p.Glu495Gly
ENST00000415930.7:c.1517A>G	ENSP00000405573.2:p.Glu506Gly
ENST00000586077.1:n.2446A>G
ENST00000586392.1:n.1222A>G
ENST00000586425.1:c.1399-173A>G	ENSP00000467670.2:n.1399-173A>G
ENST00000588991.6:c.1529A>G	ENSP00000465858.2:p.Glu510Gly
ENST00000592740.5:c.193+3071A>G
NM_000175.3:c.1484A>G	NP_000166.2:p.Glu495Gly
NM_001184722.1:c.1517A>G	NP_001171651.1:p.Glu506Gly
NM_001289789.1:c.1601A>G	NP_001276718.1:p.Glu534Gly
NM_001289790.1:c.1400A>G	NP_001276719.1:p.Glu467Gly
XM_005258764.1:c.1484A>G	XP_005258821.1:p.Glu495Gly
XM_006723148.1:c.1484A>G	XP_006723211.1:p.Glu495Gly
XM_011526754.1:c.1601A>G	XP_011525056.1:p.Glu534Gly
NM_000175.5:c.1484A>G MANE Select	NP_000166.2:p.Glu495Gly
NM_001289790.2:c.1400A>G	NP_001276719.1:p.Glu467Gly
NM_001329909.1:c.1484A>G	NP_001316838.1:p.Glu495Gly
NM_001329910.1:c.1484A>G	NP_001316839.1:p.Glu495Gly
NM_001329911.1:c.1457A>G	NP_001316840.1:p.Glu486Gly
XM_011526754.3:c.1601A>G	XP_011525056.1:p.Glu534Gly
NM_001289790.3:c.1400A>G	NP_001276719.1:p.Glu467Gly
NM_001329911.2:c.1457A>G	NP_001316840.1:p.Glu486Gly