Canonical Allele Identifier: CA2333167599

Gene: GPI

Linked Data

• dbSNP Id: rs2074594932

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34378895del , CM000681.2:g.34378895del	GRCh38
NC_000019.9:g.34869800del , CM000681.1:g.34869800del	GRCh37
NC_000019.8:g.39561640del	NCBI36
NG_012838.2:g.19156del
NG_012838.3:g.24304del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.634-39del MANE Select	ENSP00000348877.3:n.634-39del
ENST00000415930.8:c.751-39del	ENSP00000405573.3:n.751-39del
ENST00000586425.2:c.522-39del
ENST00000588991.7:c.667-39del	ENSP00000465858.3:n.667-39del
ENST00000589399.6:c.403-39del	ENSP00000468201.2:n.403-39del
ENST00000643067.1:n.1144-39del
ENST00000647446.1:c.634-39del	ENSP00000495129.1:n.634-39del
ENST00000356487.9:c.634-39del	ENSP00000348877.3:n.634-39del
ENST00000415930.7:c.667-39del	ENSP00000405573.2:n.667-39del
ENST00000586425.1:c.634-39del	ENSP00000467670.2:n.634-39del
ENST00000588991.6:c.679-39del	ENSP00000465858.2:n.679-39del
NM_000175.3:c.634-39del	NP_000166.2:n.634-39del
NM_001184722.1:c.667-39del	NP_001171651.1:n.667-39del
NM_001289789.1:c.751-39del	NP_001276718.1:n.751-39del
NM_001289790.1:c.550-39del	NP_001276719.1:n.550-39del
XM_005258764.1:c.634-39del	XP_005258821.1:n.634-39del
XM_006723148.1:c.634-39del	XP_006723211.1:n.634-39del
XM_011526754.1:c.751-39del	XP_011525056.1:n.751-39del
XM_011526755.1:c.751-39del	XP_011525057.1:n.751-39del
NM_000175.5:c.634-39del MANE Select	NP_000166.2:n.634-39del
NM_001289790.2:c.550-39del	NP_001276719.1:n.550-39del
NM_001329909.1:c.634-39del	NP_001316838.1:n.634-39del
NM_001329910.1:c.634-39del	NP_001316839.1:n.634-39del
NM_001329911.1:c.634-39del	NP_001316840.1:n.634-39del
XM_011526754.3:c.751-39del	XP_011525056.1:n.751-39del
NM_001289790.3:c.550-39del	NP_001276719.1:n.550-39del
NM_001329911.2:c.634-39del	NP_001316840.1:n.634-39del