Canonical Allele Identifier: CA9367479

Gene: GPI

Linked Data

• dbSNP Id: rs755615286
• ExAC: 19:34890779 T / TCTTCC
• gnomAD v2: 19-34890779-T-TCTTCC
• gnomAD v4: 19-34399874-T-TCTTCC
• MyVariant Identifiers: chr19:g.34890784_34890785insCTTCC (hg19) ; chr19:g.34890779_34890780insCTTCC (hg19) ; chr19:g.34399874_34399875insCTTCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399889_34399893dup , CM000681.2:g.34399889_34399893dup	GRCh38
NC_000019.9:g.34890794_34890798dup , CM000681.1:g.34890794_34890798dup	GRCh37
NC_000019.8:g.39582634_39582638dup	NCBI36
NG_012838.2:g.40150_40154dup
NG_012838.3:g.45298_45302dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1542-12_1542-8dup MANE Select	ENSP00000348877.3:n.1542-12_1542-8dup
ENST00000415930.8:c.1659-12_1659-8dup	ENSP00000405573.3:n.1659-12_1659-8dup
ENST00000586425.2:c.1208-12_1208-8dup
ENST00000588991.7:c.1575-12_1575-8dup	ENSP00000465858.3:n.1575-12_1575-8dup
ENST00000643067.1:n.2587-12_2587-8dup
ENST00000647446.1:c.*593-12_*593-8dup	ENSP00000495129.1:n.*593-12_*593-8dup
ENST00000356487.9:c.1542-12_1542-8dup	ENSP00000348877.3:n.1542-12_1542-8dup
ENST00000415930.7:c.1575-12_1575-8dup	ENSP00000405573.2:n.1575-12_1575-8dup
ENST00000586077.1:n.2607_2611dup
ENST00000586392.1:n.1280-12_1280-8dup
ENST00000586425.1:c.1399-12_1399-8dup	ENSP00000467670.2:n.1399-12_1399-8dup
ENST00000588991.6:c.1587-12_1587-8dup	ENSP00000465858.2:n.1587-12_1587-8dup
ENST00000592740.5:c.193+3232_193+3236dup
NM_000175.3:c.1542-12_1542-8dup	NP_000166.2:n.1542-12_1542-8dup
NM_001184722.1:c.1575-12_1575-8dup	NP_001171651.1:n.1575-12_1575-8dup
NM_001289789.1:c.1659-12_1659-8dup	NP_001276718.1:n.1659-12_1659-8dup
NM_001289790.1:c.1458-12_1458-8dup	NP_001276719.1:n.1458-12_1458-8dup
XM_005258764.1:c.1542-12_1542-8dup	XP_005258821.1:n.1542-12_1542-8dup
XM_006723148.1:c.1542-12_1542-8dup	XP_006723211.1:n.1542-12_1542-8dup
XM_011526754.1:c.1659-12_1659-8dup	XP_011525056.1:n.1659-12_1659-8dup
NM_000175.5:c.1542-12_1542-8dup MANE Select	NP_000166.2:n.1542-12_1542-8dup
NM_001289790.2:c.1458-12_1458-8dup	NP_001276719.1:n.1458-12_1458-8dup
NM_001329909.1:c.1542-12_1542-8dup	NP_001316838.1:n.1542-12_1542-8dup
NM_001329910.1:c.1542-12_1542-8dup	NP_001316839.1:n.1542-12_1542-8dup
NM_001329911.1:c.1515-12_1515-8dup	NP_001316840.1:n.1515-12_1515-8dup
XM_011526754.3:c.1659-12_1659-8dup	XP_011525056.1:n.1659-12_1659-8dup
NM_001289790.3:c.1458-12_1458-8dup	NP_001276719.1:n.1458-12_1458-8dup
NM_001329911.2:c.1515-12_1515-8dup	NP_001316840.1:n.1515-12_1515-8dup