Canonical Allele Identifier: CA2814215043

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399786_34399900del , CM000681.2:g.34399786_34399900del	GRCh38
NC_000019.9:g.34890691_34890805del , CM000681.1:g.34890691_34890805del	GRCh37
NC_000019.8:g.39582531_39582645del	NCBI36
NG_012838.2:g.40047_40161del
NG_012838.3:g.45195_45309del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1541+1_1542-1del
ENST00000415930.8:c.1658+1_1659-1del
ENST00000586425.2:c.1207+1_1208-1del
ENST00000588991.7:c.1574+1_1575-1del
ENST00000643067.1:n.2586+1_2587-1del
ENST00000647446.1:c.*592+1_*593-1del
ENST00000356487.9:c.1541+1_1542-1del
ENST00000415930.7:c.1574+1_1575-1del
ENST00000586077.1:n.2504_2618del
ENST00000586392.1:n.1279+1_1280-1del
ENST00000586425.1:c.1399-115_1399-1del	ENSP00000467670.2:n.1399-115_1399-1del
ENST00000588991.6:c.1586+1_1587-1del
ENST00000592740.5:c.193+3129_193+3243del
NM_000175.3:c.1541+1_1542-1del
NM_001184722.1:c.1574+1_1575-1del
NM_001289789.1:c.1658+1_1659-1del
NM_001289790.1:c.1457+1_1458-1del
XM_005258764.1:c.1541+1_1542-1del
XM_006723148.1:c.1541+1_1542-1del
XM_011526754.1:c.1658+1_1659-1del
NM_000175.5:c.1541+1_1542-1del
NM_001289790.2:c.1457+1_1458-1del
NM_001329909.1:c.1541+1_1542-1del
NM_001329910.1:c.1541+1_1542-1del
NM_001329911.1:c.1514+1_1515-1del
XM_011526754.3:c.1658+1_1659-1del
NM_001289790.3:c.1457+1_1458-1del
NM_001329911.2:c.1514+1_1515-1del