Canonical Allele Identifier: CA9367132

Gene: GPI

Linked Data

• dbSNP Id: rs772613140
• ExAC: 19:34869797 C / A
• gnomAD v2: 19-34869797-C-A
• gnomAD v4: 19-34378892-C-A
• MyVariant Identifiers: chr19:g.34869797C>A (hg19) ; chr19:g.34378892C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34378892C>A , CM000681.2:g.34378892C>A	GRCh38
NC_000019.9:g.34869797C>A , CM000681.1:g.34869797C>A	GRCh37
NC_000019.8:g.39561637C>A	NCBI36
NG_012838.2:g.19153C>A
NG_012838.3:g.24301C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356487.11:c.634-42C>A MANE Select	ENSP00000348877.3:n.634-42C>A
ENST00000415930.8:c.751-42C>A	ENSP00000405573.3:n.751-42C>A
ENST00000586425.2:c.522-42C>A
ENST00000588991.7:c.667-42C>A	ENSP00000465858.3:n.667-42C>A
ENST00000589399.6:c.403-42C>A	ENSP00000468201.2:n.403-42C>A
ENST00000643067.1:n.1144-42C>A
ENST00000647446.1:c.634-42C>A	ENSP00000495129.1:n.634-42C>A
ENST00000356487.9:c.634-42C>A	ENSP00000348877.3:n.634-42C>A
ENST00000415930.7:c.667-42C>A	ENSP00000405573.2:n.667-42C>A
ENST00000586425.1:c.634-42C>A	ENSP00000467670.2:n.634-42C>A
ENST00000588991.6:c.679-42C>A	ENSP00000465858.2:n.679-42C>A
NM_000175.3:c.634-42C>A	NP_000166.2:n.634-42C>A
NM_001184722.1:c.667-42C>A	NP_001171651.1:n.667-42C>A
NM_001289789.1:c.751-42C>A	NP_001276718.1:n.751-42C>A
NM_001289790.1:c.550-42C>A	NP_001276719.1:n.550-42C>A
XM_005258764.1:c.634-42C>A	XP_005258821.1:n.634-42C>A
XM_006723148.1:c.634-42C>A	XP_006723211.1:n.634-42C>A
XM_011526754.1:c.751-42C>A	XP_011525056.1:n.751-42C>A
XM_011526755.1:c.751-42C>A	XP_011525057.1:n.751-42C>A
NM_000175.5:c.634-42C>A MANE Select	NP_000166.2:n.634-42C>A
NM_001289790.2:c.550-42C>A	NP_001276719.1:n.550-42C>A
NM_001329909.1:c.634-42C>A	NP_001316838.1:n.634-42C>A
NM_001329910.1:c.634-42C>A	NP_001316839.1:n.634-42C>A
NM_001329911.1:c.634-42C>A	NP_001316840.1:n.634-42C>A
XM_011526754.3:c.751-42C>A	XP_011525056.1:n.751-42C>A
NM_001289790.3:c.550-42C>A	NP_001276719.1:n.550-42C>A
NM_001329911.2:c.634-42C>A	NP_001316840.1:n.634-42C>A