Canonical Allele Identifier: CA2580096797

Gene: GPI

Linked Data

• ClinVar Variation Id: 1701363
• ClinVar RCV Id: RCV002276413
• dbSNP Id: rs2145438228

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399894_34399895delinsCC , CM000681.2:g.34399894_34399895delinsCC	GRCh38
NC_000019.9:g.34890799_34890800delinsCC , CM000681.1:g.34890799_34890800delinsCC	GRCh37
NC_000019.8:g.39582639_39582640delinsCC	NCBI36
NG_012838.2:g.40155_40156delinsCC
NG_012838.3:g.45303_45304delinsCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000356487.11:c.1542-7_1542-6delinsCC MANE Select	ENSP00000348877.3:n.1542-7_1542-6delinsCC...
ENST00000415930.8:c.1659-7_1659-6delinsCC	ENSP00000405573.3:n.1659-7_1659-6delinsCC...
ENST00000586425.2:c.1208-7_1208-6delinsCC
ENST00000588991.7:c.1575-7_1575-6delinsCC	ENSP00000465858.3:n.1575-7_1575-6delinsCC...
ENST00000643067.1:n.2587-7_2587-6delinsCC
ENST00000647446.1:c.*593-7_*593-6delinsCC	ENSP00000495129.1:n.*593-7_*593-6delinsCC...
ENST00000356487.9:c.1542-7_1542-6delinsCC	ENSP00000348877.3:n.1542-7_1542-6delinsCC...
ENST00000415930.7:c.1575-7_1575-6delinsCC	ENSP00000405573.2:n.1575-7_1575-6delinsCC...
ENST00000586077.1:n.2612_2613delinsCC
ENST00000586392.1:n.1280-7_1280-6delinsCC
ENST00000586425.1:c.1399-7_1399-6delinsCC	ENSP00000467670.2:n.1399-7_1399-6delinsCC...
ENST00000588991.6:c.1587-7_1587-6delinsCC	ENSP00000465858.2:n.1587-7_1587-6delinsCC...
ENST00000592740.5:c.193+3237_193+3238delinsCC
NM_000175.3:c.1542-7_1542-6delinsCC	NP_000166.2:n.1542-7_1542-6delinsCC
NM_001184722.1:c.1575-7_1575-6delinsCC	NP_001171651.1:n.1575-7_1575-6delinsCC
NM_001289789.1:c.1659-7_1659-6delinsCC	NP_001276718.1:n.1659-7_1659-6delinsCC
NM_001289790.1:c.1458-7_1458-6delinsCC	NP_001276719.1:n.1458-7_1458-6delinsCC
XM_005258764.1:c.1542-7_1542-6delinsCC	XP_005258821.1:n.1542-7_1542-6delinsCC
XM_006723148.1:c.1542-7_1542-6delinsCC	XP_006723211.1:n.1542-7_1542-6delinsCC
XM_011526754.1:c.1659-7_1659-6delinsCC	XP_011525056.1:n.1659-7_1659-6delinsCC
NM_000175.5:c.1542-7_1542-6delinsCC MANE Select	NP_000166.2:n.1542-7_1542-6delinsCC
NM_001289790.2:c.1458-7_1458-6delinsCC	NP_001276719.1:n.1458-7_1458-6delinsCC
NM_001329909.1:c.1542-7_1542-6delinsCC	NP_001316838.1:n.1542-7_1542-6delinsCC
NM_001329910.1:c.1542-7_1542-6delinsCC	NP_001316839.1:n.1542-7_1542-6delinsCC
NM_001329911.1:c.1515-7_1515-6delinsCC	NP_001316840.1:n.1515-7_1515-6delinsCC
XM_011526754.3:c.1659-7_1659-6delinsCC	XP_011525056.1:n.1659-7_1659-6delinsCC
NM_001289790.3:c.1458-7_1458-6delinsCC	NP_001276719.1:n.1458-7_1458-6delinsCC
NM_001329911.2:c.1515-7_1515-6delinsCC	NP_001316840.1:n.1515-7_1515-6delinsCC