Canonical Allele Identifier: CA2587871747

Gene: C3

Linked Data

• gnomAD v4: 19-6679274-G-GGCCACACCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679274_6679275insGCCACACCCA , CM000681.2:g.6679274_6679275insGCCACACCCA	GRCh38
NC_000019.9:g.6679285_6679286insGCCACACCCA , CM000681.1:g.6679285_6679286insGCCACACCCA	GRCh37
NC_000019.8:g.6630285_6630286insGCCACACCCA	NCBI36
NG_009557.1:g.46377_46378insTGGGTGTGGC , LRG_27:g.46377_46378insTGGGTGTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2895-67_2895-66insTGGGTGTGGC
ENST00000695653.1:c.2456-67_2456-66insTGGGTGTGGC	ENSP00000512084.1:n.2456-67_2456-66insTGGGTGTGGC
ENST00000695654.1:c.3572-67_3572-66insTGGGTGTGGC	ENSP00000512085.1:n.3572-67_3572-66insTGGGTGTGGC
ENST00000695689.1:c.518-67_518-66insTGGGTGTGGC	ENSP00000512101.1:n.518-67_518-66insTGGGTGTGGC
ENST00000695690.1:n.1612-67_1612-66insTGGGTGTGGC
ENST00000695691.1:n.1408-67_1408-66insTGGGTGTGGC
ENST00000245907.11:c.4547-67_4547-66insTGGGTGTGGC MANE Select	ENSP00000245907.4:n.4547-67_4547-66insTGGGTGTGGC
ENST00000245907.10:c.4547-67_4547-66insTGGGTGTGGC	ENSP00000245907.4:n.4547-67_4547-66insTGGGTGTGGC
ENST00000599668.1:n.167-67_167-66insTGGGTGTGGC
ENST00000599899.5:n.1506-67_1506-66insTGGGTGTGGC
ENST00000601008.1:c.242-1317_242-1316insTGGGTGTGGC	ENSP00000471384.1:n.242-1317_242-1316insTGGGTGTGGC
NM_000064.3:c.4547-67_4547-66insTGGGTGTGGC	NP_000055.2:n.4547-67_4547-66insTGGGTGTGGC
NM_000064.4:c.4547-67_4547-66insTGGGTGTGGC MANE Select	NP_000055.2:n.4547-67_4547-66insTGGGTGTGGC