Canonical Allele Identifier: CA920098798

Gene: GPI

Linked Data

• dbSNP Id: rs1568352374
• gnomAD v4: 19-34400028-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34400029del , CM000681.2:g.34400029del	GRCh38
NC_000019.9:g.34890934del , CM000681.1:g.34890934del	GRCh37
NC_000019.8:g.39582774del	NCBI36
NG_012838.2:g.40290del
NG_012838.3:g.45438del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1670del MANE Select	ENSP00000348877.3:p.Val557AlafsTer?
ENST00000415930.8:c.1787del	ENSP00000405573.3:p.Val596AlafsTer?
ENST00000586425.2:c.1336del
ENST00000588991.7:c.1703del	ENSP00000465858.3:p.Val568AlafsTer?
ENST00000643067.1:n.2715del
ENST00000647446.1:c.*721del	ENSP00000495129.1:n.*721del
ENST00000356487.9:c.1670del	ENSP00000348877.3:p.Val557AlafsTer?
ENST00000415930.7:c.1703del	ENSP00000405573.2:p.Val568AlafsTer?
ENST00000586077.1:n.2747del
ENST00000586392.1:n.1408del
ENST00000586425.1:c.*102del	ENSP00000467670.2:n.*102del
ENST00000588991.6:c.1715del	ENSP00000465858.2:p.Val572AlafsTer?
ENST00000592740.5:c.193+3372del
NM_000175.3:c.1670del	NP_000166.2:p.Val557AlafsTer?
NM_001184722.1:c.1703del	NP_001171651.1:p.Val568AlafsTer?
NM_001289789.1:c.1787del	NP_001276718.1:p.Val596AlafsTer?
NM_001289790.1:c.1586del	NP_001276719.1:p.Val529AlafsTer?
XM_005258764.1:c.1670del	XP_005258821.1:p.Val557AlafsTer?
XM_006723148.1:c.1670del	XP_006723211.1:p.Val557AlafsTer?
XM_011526754.1:c.1787del	XP_011525056.1:p.Val596AlafsTer?
NM_000175.5:c.1670del MANE Select	NP_000166.2:p.Val557AlafsTer?
NM_001289790.2:c.1586del	NP_001276719.1:p.Val529AlafsTer?
NM_001329909.1:c.1670del	NP_001316838.1:p.Val557AlafsTer?
NM_001329910.1:c.1670del	NP_001316839.1:p.Val557AlafsTer?
NM_001329911.1:c.1643del	NP_001316840.1:p.Val548AlafsTer?
XM_011526754.3:c.1787del	XP_011525056.1:p.Val596AlafsTer?
NM_001289790.3:c.1586del	NP_001276719.1:p.Val529AlafsTer?
NM_001329911.2:c.1643del	NP_001316840.1:p.Val548AlafsTer?