Canonical Allele Identifier: CA9367497

Gene: GPI

Linked Data

• dbSNP Id: rs764328500
• ExAC: 19:34890892 A / G
• gnomAD v2: 19-34890892-A-G
• gnomAD v4: 19-34399987-A-G
• MyVariant Identifiers: chr19:g.34890892A>G (hg19) ; chr19:g.34399987A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399987A>G , CM000681.2:g.34399987A>G	GRCh38
NC_000019.9:g.34890892A>G , CM000681.1:g.34890892A>G	GRCh37
NC_000019.8:g.39582732A>G	NCBI36
NG_012838.2:g.40248A>G
NG_012838.3:g.45396A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356487.11:c.1628A>G MANE Select	ENSP00000348877.3:p.Asn543Ser
ENST00000415930.8:c.1745A>G	ENSP00000405573.3:p.Asn582Ser
ENST00000586425.2:c.1294A>G
ENST00000588991.7:c.1661A>G	ENSP00000465858.3:p.Asn554Ser
ENST00000643067.1:n.2673A>G
ENST00000647446.1:c.*679A>G	ENSP00000495129.1:n.*679A>G
ENST00000356487.9:c.1628A>G	ENSP00000348877.3:p.Asn543Ser
ENST00000415930.7:c.1661A>G	ENSP00000405573.2:p.Asn554Ser
ENST00000586077.1:n.2705A>G
ENST00000586392.1:n.1366A>G
ENST00000586425.1:c.*60A>G	ENSP00000467670.2:n.*60A>G
ENST00000588991.6:c.1673A>G	ENSP00000465858.2:p.Asn558Ser
ENST00000592740.5:c.193+3330A>G
NM_000175.3:c.1628A>G	NP_000166.2:p.Asn543Ser
NM_001184722.1:c.1661A>G	NP_001171651.1:p.Asn554Ser
NM_001289789.1:c.1745A>G	NP_001276718.1:p.Asn582Ser
NM_001289790.1:c.1544A>G	NP_001276719.1:p.Asn515Ser
XM_005258764.1:c.1628A>G	XP_005258821.1:p.Asn543Ser
XM_006723148.1:c.1628A>G	XP_006723211.1:p.Asn543Ser
XM_011526754.1:c.1745A>G	XP_011525056.1:p.Asn582Ser
NM_000175.5:c.1628A>G MANE Select	NP_000166.2:p.Asn543Ser
NM_001289790.2:c.1544A>G	NP_001276719.1:p.Asn515Ser
NM_001329909.1:c.1628A>G	NP_001316838.1:p.Asn543Ser
NM_001329910.1:c.1628A>G	NP_001316839.1:p.Asn543Ser
NM_001329911.1:c.1601A>G	NP_001316840.1:p.Asn534Ser
XM_011526754.3:c.1745A>G	XP_011525056.1:p.Asn582Ser
NM_001289790.3:c.1544A>G	NP_001276719.1:p.Asn515Ser
NM_001329911.2:c.1601A>G	NP_001316840.1:p.Asn534Ser