Canonical Allele Identifier: CA9367464

Gene: GPI

Linked Data

• dbSNP Id: rs771403151
• ExAC: 19:34890716 C / T
• gnomAD v2: 19-34890716-C-T
• gnomAD v4: 19-34399811-C-T
• MyVariant Identifiers: chr19:g.34890716C>T (hg19) ; chr19:g.34399811C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399811C>T , CM000681.2:g.34399811C>T	GRCh38
NC_000019.9:g.34890716C>T , CM000681.1:g.34890716C>T	GRCh37
NC_000019.8:g.39582556C>T	NCBI36
NG_012838.2:g.40072C>T
NG_012838.3:g.45220C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1541+26C>T MANE Select	ENSP00000348877.3:n.1541+26C>T
ENST00000415930.8:c.1658+26C>T	ENSP00000405573.3:n.1658+26C>T
ENST00000586425.2:c.1207+26C>T
ENST00000588991.7:c.1574+26C>T	ENSP00000465858.3:n.1574+26C>T
ENST00000643067.1:n.2586+26C>T
ENST00000647446.1:c.*592+26C>T	ENSP00000495129.1:n.*592+26C>T
ENST00000356487.9:c.1541+26C>T	ENSP00000348877.3:n.1541+26C>T
ENST00000415930.7:c.1574+26C>T	ENSP00000405573.2:n.1574+26C>T
ENST00000586077.1:n.2529C>T
ENST00000586392.1:n.1279+26C>T
ENST00000586425.1:c.1399-90C>T	ENSP00000467670.2:n.1399-90C>T
ENST00000588991.6:c.1586+26C>T	ENSP00000465858.2:n.1586+26C>T
ENST00000592740.5:c.193+3154C>T
NM_000175.3:c.1541+26C>T	NP_000166.2:n.1541+26C>T
NM_001184722.1:c.1574+26C>T	NP_001171651.1:n.1574+26C>T
NM_001289789.1:c.1658+26C>T	NP_001276718.1:n.1658+26C>T
NM_001289790.1:c.1457+26C>T	NP_001276719.1:n.1457+26C>T
XM_005258764.1:c.1541+26C>T	XP_005258821.1:n.1541+26C>T
XM_006723148.1:c.1541+26C>T	XP_006723211.1:n.1541+26C>T
XM_011526754.1:c.1658+26C>T	XP_011525056.1:n.1658+26C>T
NM_000175.5:c.1541+26C>T MANE Select	NP_000166.2:n.1541+26C>T
NM_001289790.2:c.1457+26C>T	NP_001276719.1:n.1457+26C>T
NM_001329909.1:c.1541+26C>T	NP_001316838.1:n.1541+26C>T
NM_001329910.1:c.1541+26C>T	NP_001316839.1:n.1541+26C>T
NM_001329911.1:c.1514+26C>T	NP_001316840.1:n.1514+26C>T
XM_011526754.3:c.1658+26C>T	XP_011525056.1:n.1658+26C>T
NM_001289790.3:c.1457+26C>T	NP_001276719.1:n.1457+26C>T
NM_001329911.2:c.1514+26C>T	NP_001316840.1:n.1514+26C>T