Canonical Allele Identifier: CA405246439

Gene: GPI

Linked Data

• MyVariant Identifiers: chr19:g.34890646C>G (hg19) ; chr19:g.34399741C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399741C>G , CM000681.2:g.34399741C>G	GRCh38
NC_000019.9:g.34890646C>G , CM000681.1:g.34890646C>G	GRCh37
NC_000019.8:g.39582486C>G	NCBI36
NG_012838.2:g.40002C>G
NG_012838.3:g.45150C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1497C>G MANE Select	ENSP00000348877.3:p.Phe499Leu
ENST00000415930.8:c.1614C>G	ENSP00000405573.3:p.Phe538Leu
ENST00000586425.2:c.1163C>G
ENST00000588991.7:c.1530C>G	ENSP00000465858.3:p.Phe510Leu
ENST00000643067.1:n.2542C>G
ENST00000647446.1:c.*548C>G	ENSP00000495129.1:n.*548C>G
ENST00000356487.9:c.1497C>G	ENSP00000348877.3:p.Phe499Leu
ENST00000415930.7:c.1530C>G	ENSP00000405573.2:p.Phe510Leu
ENST00000586077.1:n.2459C>G
ENST00000586392.1:n.1235C>G
ENST00000586425.1:c.1399-160C>G	ENSP00000467670.2:n.1399-160C>G
ENST00000588991.6:c.1542C>G	ENSP00000465858.2:p.Phe514Leu
ENST00000592740.5:c.193+3084C>G
NM_000175.3:c.1497C>G	NP_000166.2:p.Phe499Leu
NM_001184722.1:c.1530C>G	NP_001171651.1:p.Phe510Leu
NM_001289789.1:c.1614C>G	NP_001276718.1:p.Phe538Leu
NM_001289790.1:c.1413C>G	NP_001276719.1:p.Phe471Leu
XM_005258764.1:c.1497C>G	XP_005258821.1:p.Phe499Leu
XM_006723148.1:c.1497C>G	XP_006723211.1:p.Phe499Leu
XM_011526754.1:c.1614C>G	XP_011525056.1:p.Phe538Leu
NM_000175.5:c.1497C>G MANE Select	NP_000166.2:p.Phe499Leu
NM_001289790.2:c.1413C>G	NP_001276719.1:p.Phe471Leu
NM_001329909.1:c.1497C>G	NP_001316838.1:p.Phe499Leu
NM_001329910.1:c.1497C>G	NP_001316839.1:p.Phe499Leu
NM_001329911.1:c.1470C>G	NP_001316840.1:p.Phe490Leu
XM_011526754.3:c.1614C>G	XP_011525056.1:p.Phe538Leu
NM_001289790.3:c.1413C>G	NP_001276719.1:p.Phe471Leu
NM_001329911.2:c.1470C>G	NP_001316840.1:p.Phe490Leu