Canonical Allele Identifier: CA9367494

Gene: GPI

Linked Data

• dbSNP Id: rs766494581
• ExAC: 19:34890881 C / T
• gnomAD v2: 19-34890881-C-T
• gnomAD v4: 19-34399976-C-T
• MyVariant Identifiers: chr19:g.34890881C>T (hg19) ; chr19:g.34399976C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399976C>T , CM000681.2:g.34399976C>T	GRCh38
NC_000019.9:g.34890881C>T , CM000681.1:g.34890881C>T	GRCh37
NC_000019.8:g.39582721C>T	NCBI36
NG_012838.2:g.40237C>T
NG_012838.3:g.45385C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356487.11:c.1617C>T MANE Select	ENSP00000348877.3:p.Asp539=
ENST00000415930.8:c.1734C>T	ENSP00000405573.3:p.Asp578=
ENST00000586425.2:c.1283C>T
ENST00000588991.7:c.1650C>T	ENSP00000465858.3:p.Asp550=
ENST00000643067.1:n.2662C>T
ENST00000647446.1:c.*668C>T	ENSP00000495129.1:n.*668C>T
ENST00000356487.9:c.1617C>T	ENSP00000348877.3:p.Asp539=
ENST00000415930.7:c.1650C>T	ENSP00000405573.2:p.Asp550=
ENST00000586077.1:n.2694C>T
ENST00000586392.1:n.1355C>T
ENST00000586425.1:c.*49C>T	ENSP00000467670.2:n.*49C>T
ENST00000588991.6:c.1662C>T	ENSP00000465858.2:p.Asp554=
ENST00000592740.5:c.193+3319C>T
NM_000175.3:c.1617C>T	NP_000166.2:p.Asp539=
NM_001184722.1:c.1650C>T	NP_001171651.1:p.Asp550=
NM_001289789.1:c.1734C>T	NP_001276718.1:p.Asp578=
NM_001289790.1:c.1533C>T	NP_001276719.1:p.Asp511=
XM_005258764.1:c.1617C>T	XP_005258821.1:p.Asp539=
XM_006723148.1:c.1617C>T	XP_006723211.1:p.Asp539=
XM_011526754.1:c.1734C>T	XP_011525056.1:p.Asp578=
NM_000175.5:c.1617C>T MANE Select	NP_000166.2:p.Asp539=
NM_001289790.2:c.1533C>T	NP_001276719.1:p.Asp511=
NM_001329909.1:c.1617C>T	NP_001316838.1:p.Asp539=
NM_001329910.1:c.1617C>T	NP_001316839.1:p.Asp539=
NM_001329911.1:c.1590C>T	NP_001316840.1:p.Asp530=
XM_011526754.3:c.1734C>T	XP_011525056.1:p.Asp578=
NM_001289790.3:c.1533C>T	NP_001276719.1:p.Asp511=
NM_001329911.2:c.1590C>T	NP_001316840.1:p.Asp530=