Canonical Allele Identifier: CA2814215037
Gene: GPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.34399632_34399718del , CM000681.2:g.34399632_34399718del GRCh38
NC_000019.9:g.34890537_34890623del , CM000681.1:g.34890537_34890623del GRCh37
NC_000019.8:g.39582377_39582463del NCBI36
NG_012838.2:g.39893_39979del
NG_012838.3:g.45041_45127del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356487.11:c.1474+1_1475-1del
ENST00000415930.8:c.1591+1_1592-1del
ENST00000586425.2:c.1158-104_1158-18del
ENST00000588991.7:c.1507+1_1508-1del
ENST00000643067.1:n.2519+1_2520-1del
ENST00000647446.1:c.*525+1_*526-1del
ENST00000356487.9:c.1474+1_1475-1del
ENST00000415930.7:c.1507+1_1508-1del
ENST00000586077.1:n.2350_2436del
ENST00000586392.1:n.1212+1_1213-1del
ENST00000586425.1:c.1399-269_1399-183del ENSP00000467670.2:n.1399-269_1399-183del
ENST00000588991.6:c.1519+1_1520-1del
ENST00000592740.5:c.193+2975_193+3061del
NM_000175.3:c.1474+1_1475-1del
NM_001184722.1:c.1507+1_1508-1del
NM_001289789.1:c.1591+1_1592-1del
NM_001289790.1:c.1390+1_1391-1del
XM_005258764.1:c.1474+1_1475-1del
XM_006723148.1:c.1474+1_1475-1del
XM_011526754.1:c.1591+1_1592-1del
NM_000175.5:c.1474+1_1475-1del
NM_001289790.2:c.1390+1_1391-1del
NM_001329909.1:c.1474+1_1475-1del
NM_001329910.1:c.1474+1_1475-1del
NM_001329911.1:c.1447+1_1448-1del
XM_011526754.3:c.1591+1_1592-1del
NM_001289790.3:c.1390+1_1391-1del
NM_001329911.2:c.1447+1_1448-1del