Canonical Allele Identifier: CA2832565459

Gene: GPI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1541+1dup
ENST00000415930.8:c.1658+1dup
ENST00000586425.2:c.1207+1dup
ENST00000588991.7:c.1574+1dup
ENST00000643067.1:n.2586+1dup
ENST00000647446.1:c.*592+1dup
ENST00000356487.9:c.1541+1dup
ENST00000415930.7:c.1574+1dup
ENST00000586077.1:n.2504dup
ENST00000586392.1:n.1279+1dup
ENST00000586425.1:c.1399-115dup	ENSP00000467670.2:n.1399-115dup
ENST00000588991.6:c.1586+1dup
ENST00000592740.5:c.193+3129dup
NM_000175.3:c.1541+1dup
NM_001184722.1:c.1574+1dup
NM_001289789.1:c.1658+1dup
NM_001289790.1:c.1457+1dup
XM_005258764.1:c.1541+1dup
XM_006723148.1:c.1541+1dup
XM_011526754.1:c.1658+1dup
NM_000175.5:c.1541+1dup
NM_001289790.2:c.1457+1dup
NM_001329909.1:c.1541+1dup
NM_001329910.1:c.1541+1dup
NM_001329911.1:c.1514+1dup
XM_011526754.3:c.1658+1dup
NM_001289790.3:c.1457+1dup
NM_001329911.2:c.1514+1dup