Canonical Allele Identifier: CA2695228519

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399630_34399633del , CM000681.2:g.34399630_34399633del	GRCh38
NC_000019.9:g.34890535_34890538del , CM000681.1:g.34890535_34890538del	GRCh37
NC_000019.8:g.39582375_39582378del	NCBI36
NG_012838.2:g.39891_39894del
NG_012838.3:g.45039_45042del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1473_1474+2del
ENST00000415930.8:c.1590_1591+2del
ENST00000586425.2:c.1158-106_1158-103del
ENST00000588991.7:c.1506_1507+2del
ENST00000643067.1:n.2518_2519+2del
ENST00000647446.1:c.*524_*525+2del
ENST00000356487.9:c.1473_1474+2del
ENST00000415930.7:c.1506_1507+2del
ENST00000586077.1:n.2348_2351del
ENST00000586392.1:n.1211_1212+2del
ENST00000586425.1:c.1399-271_1399-268del	ENSP00000467670.2:n.1399-271_1399-268del
ENST00000588991.6:c.1518_1519+2del
ENST00000592740.5:c.193+2973_193+2976del
NM_000175.3:c.1473_1474+2del
NM_001184722.1:c.1506_1507+2del
NM_001289789.1:c.1590_1591+2del
NM_001289790.1:c.1389_1390+2del
XM_005258764.1:c.1473_1474+2del
XM_006723148.1:c.1473_1474+2del
XM_011526754.1:c.1590_1591+2del
NM_000175.5:c.1473_1474+2del
NM_001289790.2:c.1389_1390+2del
NM_001329909.1:c.1473_1474+2del
NM_001329910.1:c.1473_1474+2del
NM_001329911.1:c.1446_1447+2del
XM_011526754.3:c.1590_1591+2del
NM_001289790.3:c.1389_1390+2del
NM_001329911.2:c.1446_1447+2del