Canonical Allele Identifier: CA506999872

Gene: GPI

Linked Data

• MyVariant Identifiers: chr19:g.34890929C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34400024C>G , CM000681.2:g.34400024C>G	GRCh38
NC_000019.9:g.34890929C>G , CM000681.1:g.34890929C>G	GRCh37
NC_000019.8:g.39582769C>G	NCBI36
NG_012838.2:g.40285C>G
NG_012838.3:g.45433C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1665C>G MANE Select	ENSP00000348877.3:p.Ala555=
ENST00000415930.8:c.1782C>G	ENSP00000405573.3:p.Ala594=
ENST00000586425.2:c.1331C>G
ENST00000588991.7:c.1698C>G	ENSP00000465858.3:p.Ala566=
ENST00000643067.1:n.2710C>G
ENST00000647446.1:c.*716C>G	ENSP00000495129.1:n.*716C>G
ENST00000356487.9:c.1665C>G	ENSP00000348877.3:p.Ala555=
ENST00000415930.7:c.1698C>G	ENSP00000405573.2:p.Ala566=
ENST00000586077.1:n.2742C>G
ENST00000586392.1:n.1403C>G
ENST00000586425.1:c.*97C>G	ENSP00000467670.2:n.*97C>G
ENST00000588991.6:c.1710C>G	ENSP00000465858.2:p.Ala570=
ENST00000592740.5:c.193+3367C>G
NM_000175.3:c.1665C>G	NP_000166.2:p.Ala555=
NM_001184722.1:c.1698C>G	NP_001171651.1:p.Ala566=
NM_001289789.1:c.1782C>G	NP_001276718.1:p.Ala594=
NM_001289790.1:c.1581C>G	NP_001276719.1:p.Ala527=
XM_005258764.1:c.1665C>G	XP_005258821.1:p.Ala555=
XM_006723148.1:c.1665C>G	XP_006723211.1:p.Ala555=
XM_011526754.1:c.1782C>G	XP_011525056.1:p.Ala594=
NM_000175.5:c.1665C>G MANE Select	NP_000166.2:p.Ala555=
NM_001289790.2:c.1581C>G	NP_001276719.1:p.Ala527=
NM_001329909.1:c.1665C>G	NP_001316838.1:p.Ala555=
NM_001329910.1:c.1665C>G	NP_001316839.1:p.Ala555=
NM_001329911.1:c.1638C>G	NP_001316840.1:p.Ala546=
XM_011526754.3:c.1782C>G	XP_011525056.1:p.Ala594=
NM_001289790.3:c.1581C>G	NP_001276719.1:p.Ala527=
NM_001329911.2:c.1638C>G	NP_001316840.1:p.Ala546=