Canonical Allele Identifier: CA405246210

Gene: GPI

Linked Data

• MyVariant Identifiers: chr19:g.34890521C>A (hg19) ; chr19:g.34399616C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399616C>A , CM000681.2:g.34399616C>A	GRCh38
NC_000019.9:g.34890521C>A , CM000681.1:g.34890521C>A	GRCh37
NC_000019.8:g.39582361C>A	NCBI36
NG_012838.2:g.39877C>A
NG_012838.3:g.45025C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1459C>A MANE Select	ENSP00000348877.3:p.Leu487Ile
ENST00000415930.8:c.1576C>A	ENSP00000405573.3:p.Leu526Ile
ENST00000586425.2:c.1158-120C>A
ENST00000588991.7:c.1492C>A	ENSP00000465858.3:p.Leu498Ile
ENST00000643067.1:n.2504C>A
ENST00000647446.1:c.*510C>A	ENSP00000495129.1:n.*510C>A
ENST00000356487.9:c.1459C>A	ENSP00000348877.3:p.Leu487Ile
ENST00000415930.7:c.1492C>A	ENSP00000405573.2:p.Leu498Ile
ENST00000586077.1:n.2334C>A
ENST00000586392.1:n.1197C>A
ENST00000586425.1:c.1398+281C>A	ENSP00000467670.2:n.1398+281C>A
ENST00000588991.6:c.1504C>A	ENSP00000465858.2:p.Leu502Ile
ENST00000592740.5:c.193+2959C>A
NM_000175.3:c.1459C>A	NP_000166.2:p.Leu487Ile
NM_001184722.1:c.1492C>A	NP_001171651.1:p.Leu498Ile
NM_001289789.1:c.1576C>A	NP_001276718.1:p.Leu526Ile
NM_001289790.1:c.1375C>A	NP_001276719.1:p.Leu459Ile
XM_005258764.1:c.1459C>A	XP_005258821.1:p.Leu487Ile
XM_006723148.1:c.1459C>A	XP_006723211.1:p.Leu487Ile
XM_011526754.1:c.1576C>A	XP_011525056.1:p.Leu526Ile
NM_000175.5:c.1459C>A MANE Select	NP_000166.2:p.Leu487Ile
NM_001289790.2:c.1375C>A	NP_001276719.1:p.Leu459Ile
NM_001329909.1:c.1459C>A	NP_001316838.1:p.Leu487Ile
NM_001329910.1:c.1459C>A	NP_001316839.1:p.Leu487Ile
NM_001329911.1:c.1432C>A	NP_001316840.1:p.Leu478Ile
XM_011526754.3:c.1576C>A	XP_011525056.1:p.Leu526Ile
NM_001289790.3:c.1375C>A	NP_001276719.1:p.Leu459Ile
NM_001329911.2:c.1432C>A	NP_001316840.1:p.Leu478Ile