Canonical Allele Identifier: CA2584357543

Gene: GPI

Linked Data

• gnomAD v4: 19-34400073-TTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34400075_34400077del , CM000681.2:g.34400075_34400077del	GRCh38
NC_000019.9:g.34890980_34890982del , CM000681.1:g.34890980_34890982del	GRCh37
NC_000019.8:g.39582820_39582822del	NCBI36
NG_012838.2:g.40336_40338del
NG_012838.3:g.45484_45486del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.*39_*41del MANE Select	ENSP00000348877.3:n.*39_*41del
ENST00000415930.8:c.*39_*41del	ENSP00000405573.3:n.*39_*41del
ENST00000586425.2:c.1382_1384del
ENST00000588991.7:c.*39_*41del	ENSP00000465858.3:n.*39_*41del
ENST00000643067.1:n.2761_2763del
ENST00000647446.1:c.*767_*769del	ENSP00000495129.1:n.*767_*769del
ENST00000356487.9:c.*39_*41del	ENSP00000348877.3:n.*39_*41del
ENST00000415930.7:c.*39_*41del	ENSP00000405573.2:n.*39_*41del
ENST00000586077.1:n.2793_2795del
ENST00000586392.1:n.1454_1456del
ENST00000586425.1:c.*148_*150del	ENSP00000467670.2:n.*148_*150del
ENST00000588991.6:c.1761_1763del	ENSP00000465858.2:n.1761_1763del
ENST00000592740.5:c.193+3418_193+3420del
NM_000175.3:c.*39_*41del	NP_000166.2:n.*39_*41del
NM_001184722.1:c.*39_*41del	NP_001171651.1:n.*39_*41del
NM_001289789.1:c.*39_*41del	NP_001276718.1:n.*39_*41del
NM_001289790.1:c.*39_*41del	NP_001276719.1:n.*39_*41del
XM_005258764.1:c.*39_*41del	XP_005258821.1:n.*39_*41del
XM_006723148.1:c.*39_*41del	XP_006723211.1:n.*39_*41del
XM_011526754.1:c.*39_*41del	XP_011525056.1:n.*39_*41del
NM_000175.5:c.*39_*41del MANE Select	NP_000166.2:n.*39_*41del
NM_001289790.2:c.*39_*41del	NP_001276719.1:n.*39_*41del
NM_001329909.1:c.*39_*41del	NP_001316838.1:n.*39_*41del
NM_001329910.1:c.*39_*41del	NP_001316839.1:n.*39_*41del
NM_001329911.1:c.*39_*41del	NP_001316840.1:n.*39_*41del
XM_011526754.3:c.*39_*41del	XP_011525056.1:n.*39_*41del
NM_001289790.3:c.*39_*41del	NP_001276719.1:n.*39_*41del
NM_001329911.2:c.*39_*41del	NP_001316840.1:n.*39_*41del