Canonical Allele Identifier: CA405246168

Gene: GPI

Linked Data

• MyVariant Identifiers: chr19:g.34890515T>A (hg19) ; chr19:g.34399610T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399610T>A , CM000681.2:g.34399610T>A	GRCh38
NC_000019.9:g.34890515T>A , CM000681.1:g.34890515T>A	GRCh37
NC_000019.8:g.39582355T>A	NCBI36
NG_012838.2:g.39871T>A
NG_012838.3:g.45019T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1453T>A MANE Select	ENSP00000348877.3:p.Phe485Ile
ENST00000415930.8:c.1570T>A	ENSP00000405573.3:p.Phe524Ile
ENST00000586425.2:c.1158-126T>A
ENST00000588991.7:c.1486T>A	ENSP00000465858.3:p.Phe496Ile
ENST00000643067.1:n.2498T>A
ENST00000647446.1:c.*504T>A	ENSP00000495129.1:n.*504T>A
ENST00000356487.9:c.1453T>A	ENSP00000348877.3:p.Phe485Ile
ENST00000415930.7:c.1486T>A	ENSP00000405573.2:p.Phe496Ile
ENST00000586077.1:n.2328T>A
ENST00000586392.1:n.1191T>A
ENST00000586425.1:c.1398+275T>A	ENSP00000467670.2:n.1398+275T>A
ENST00000588991.6:c.1498T>A	ENSP00000465858.2:p.Phe500Ile
ENST00000592740.5:c.193+2953T>A
NM_000175.3:c.1453T>A	NP_000166.2:p.Phe485Ile
NM_001184722.1:c.1486T>A	NP_001171651.1:p.Phe496Ile
NM_001289789.1:c.1570T>A	NP_001276718.1:p.Phe524Ile
NM_001289790.1:c.1369T>A	NP_001276719.1:p.Phe457Ile
XM_005258764.1:c.1453T>A	XP_005258821.1:p.Phe485Ile
XM_006723148.1:c.1453T>A	XP_006723211.1:p.Phe485Ile
XM_011526754.1:c.1570T>A	XP_011525056.1:p.Phe524Ile
NM_000175.5:c.1453T>A MANE Select	NP_000166.2:p.Phe485Ile
NM_001289790.2:c.1369T>A	NP_001276719.1:p.Phe457Ile
NM_001329909.1:c.1453T>A	NP_001316838.1:p.Phe485Ile
NM_001329910.1:c.1453T>A	NP_001316839.1:p.Phe485Ile
NM_001329911.1:c.1426T>A	NP_001316840.1:p.Phe476Ile
XM_011526754.3:c.1570T>A	XP_011525056.1:p.Phe524Ile
NM_001289790.3:c.1369T>A	NP_001276719.1:p.Phe457Ile
NM_001329911.2:c.1426T>A	NP_001316840.1:p.Phe476Ile