Canonical Allele Identifier: CA506999806

Gene: GPI

Linked Data

• MyVariant Identifiers: chr19:g.34890890C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399985C>G , CM000681.2:g.34399985C>G	GRCh38
NC_000019.9:g.34890890C>G , CM000681.1:g.34890890C>G	GRCh37
NC_000019.8:g.39582730C>G	NCBI36
NG_012838.2:g.40246C>G
NG_012838.3:g.45394C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356487.11:c.1626C>G MANE Select	ENSP00000348877.3:p.Thr542=
ENST00000415930.8:c.1743C>G	ENSP00000405573.3:p.Thr581=
ENST00000586425.2:c.1292C>G
ENST00000588991.7:c.1659C>G	ENSP00000465858.3:p.Thr553=
ENST00000643067.1:n.2671C>G
ENST00000647446.1:c.*677C>G	ENSP00000495129.1:n.*677C>G
ENST00000356487.9:c.1626C>G	ENSP00000348877.3:p.Thr542=
ENST00000415930.7:c.1659C>G	ENSP00000405573.2:p.Thr553=
ENST00000586077.1:n.2703C>G
ENST00000586392.1:n.1364C>G
ENST00000586425.1:c.*58C>G	ENSP00000467670.2:n.*58C>G
ENST00000588991.6:c.1671C>G	ENSP00000465858.2:p.Thr557=
ENST00000592740.5:c.193+3328C>G
NM_000175.3:c.1626C>G	NP_000166.2:p.Thr542=
NM_001184722.1:c.1659C>G	NP_001171651.1:p.Thr553=
NM_001289789.1:c.1743C>G	NP_001276718.1:p.Thr581=
NM_001289790.1:c.1542C>G	NP_001276719.1:p.Thr514=
XM_005258764.1:c.1626C>G	XP_005258821.1:p.Thr542=
XM_006723148.1:c.1626C>G	XP_006723211.1:p.Thr542=
XM_011526754.1:c.1743C>G	XP_011525056.1:p.Thr581=
NM_000175.5:c.1626C>G MANE Select	NP_000166.2:p.Thr542=
NM_001289790.2:c.1542C>G	NP_001276719.1:p.Thr514=
NM_001329909.1:c.1626C>G	NP_001316838.1:p.Thr542=
NM_001329910.1:c.1626C>G	NP_001316839.1:p.Thr542=
NM_001329911.1:c.1599C>G	NP_001316840.1:p.Thr533=
XM_011526754.3:c.1743C>G	XP_011525056.1:p.Thr581=
NM_001289790.3:c.1542C>G	NP_001276719.1:p.Thr514=
NM_001329911.2:c.1599C>G	NP_001316840.1:p.Thr533=