Canonical Allele Identifier: CA2584357552

Gene: GPI

Linked Data

• gnomAD v4: 19-34400081-CTCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34400084_34400086del , CM000681.2:g.34400084_34400086del	GRCh38
NC_000019.9:g.34890989_34890991del , CM000681.1:g.34890989_34890991del	GRCh37
NC_000019.8:g.39582829_39582831del	NCBI36
NG_012838.2:g.40345_40347del
NG_012838.3:g.45493_45495del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.*48_*50del MANE Select	ENSP00000348877.3:n.*48_*50del
ENST00000415930.8:c.*48_*50del	ENSP00000405573.3:n.*48_*50del
ENST00000586425.2:c.1391_1393del
ENST00000588991.7:c.*48_*50del	ENSP00000465858.3:n.*48_*50del
ENST00000643067.1:n.2770_2772del
ENST00000647446.1:c.*776_*778del	ENSP00000495129.1:n.*776_*778del
ENST00000356487.9:c.*48_*50del	ENSP00000348877.3:n.*48_*50del
ENST00000415930.7:c.*48_*50del	ENSP00000405573.2:n.*48_*50del
ENST00000586077.1:n.2802_2804del
ENST00000586392.1:n.1463_1465del
ENST00000586425.1:c.*157_*159del	ENSP00000467670.2:n.*157_*159del
ENST00000588991.6:c.1770_1772del	ENSP00000465858.2:n.1770_1772del
ENST00000592740.5:c.193+3427_193+3429del
NM_000175.3:c.*48_*50del	NP_000166.2:n.*48_*50del
NM_001184722.1:c.*48_*50del	NP_001171651.1:n.*48_*50del
NM_001289789.1:c.*48_*50del	NP_001276718.1:n.*48_*50del
NM_001289790.1:c.*48_*50del	NP_001276719.1:n.*48_*50del
XM_005258764.1:c.*48_*50del	XP_005258821.1:n.*48_*50del
XM_006723148.1:c.*48_*50del	XP_006723211.1:n.*48_*50del
XM_011526754.1:c.*48_*50del	XP_011525056.1:n.*48_*50del
NM_000175.5:c.*48_*50del MANE Select	NP_000166.2:n.*48_*50del
NM_001289790.2:c.*48_*50del	NP_001276719.1:n.*48_*50del
NM_001329909.1:c.*48_*50del	NP_001316838.1:n.*48_*50del
NM_001329910.1:c.*48_*50del	NP_001316839.1:n.*48_*50del
NM_001329911.1:c.*48_*50del	NP_001316840.1:n.*48_*50del
XM_011526754.3:c.*48_*50del	XP_011525056.1:n.*48_*50del
NM_001289790.3:c.*48_*50del	NP_001276719.1:n.*48_*50del
NM_001329911.2:c.*48_*50del	NP_001316840.1:n.*48_*50del