Canonical Allele Identifier: CA2582113697

Gene: GPI

Linked Data

• gnomAD v3: 19-34399877-TC-T
• gnomAD v4: 19-34399877-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399880del , CM000681.2:g.34399880del	GRCh38
NC_000019.9:g.34890785del , CM000681.1:g.34890785del	GRCh37
NC_000019.8:g.39582625del	NCBI36
NG_012838.2:g.40141del
NG_012838.3:g.45289del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1542-21del MANE Select	ENSP00000348877.3:n.1542-21del
ENST00000415930.8:c.1659-21del	ENSP00000405573.3:n.1659-21del
ENST00000586425.2:c.1208-21del
ENST00000588991.7:c.1575-21del	ENSP00000465858.3:n.1575-21del
ENST00000643067.1:n.2587-21del
ENST00000647446.1:c.*593-21del	ENSP00000495129.1:n.*593-21del
ENST00000356487.9:c.1542-21del	ENSP00000348877.3:n.1542-21del
ENST00000415930.7:c.1575-21del	ENSP00000405573.2:n.1575-21del
ENST00000586077.1:n.2598del
ENST00000586392.1:n.1280-21del
ENST00000586425.1:c.1399-21del	ENSP00000467670.2:n.1399-21del
ENST00000588991.6:c.1587-21del	ENSP00000465858.2:n.1587-21del
ENST00000592740.5:c.193+3223del
NM_000175.3:c.1542-21del	NP_000166.2:n.1542-21del
NM_001184722.1:c.1575-21del	NP_001171651.1:n.1575-21del
NM_001289789.1:c.1659-21del	NP_001276718.1:n.1659-21del
NM_001289790.1:c.1458-21del	NP_001276719.1:n.1458-21del
XM_005258764.1:c.1542-21del	XP_005258821.1:n.1542-21del
XM_006723148.1:c.1542-21del	XP_006723211.1:n.1542-21del
XM_011526754.1:c.1659-21del	XP_011525056.1:n.1659-21del
NM_000175.5:c.1542-21del MANE Select	NP_000166.2:n.1542-21del
NM_001289790.2:c.1458-21del	NP_001276719.1:n.1458-21del
NM_001329909.1:c.1542-21del	NP_001316838.1:n.1542-21del
NM_001329910.1:c.1542-21del	NP_001316839.1:n.1542-21del
NM_001329911.1:c.1515-21del	NP_001316840.1:n.1515-21del
XM_011526754.3:c.1659-21del	XP_011525056.1:n.1659-21del
NM_001289790.3:c.1458-21del	NP_001276719.1:n.1458-21del
NM_001329911.2:c.1515-21del	NP_001316840.1:n.1515-21del