Canonical Allele Identifier: CA2320559379

Gene: C3

Linked Data

• dbSNP Id: rs1967578258

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6698025_6698026insGTA , CM000681.2:g.6698025_6698026insGTA	GRCh38
NC_000019.9:g.6698036_6698037insGTA , CM000681.1:g.6698036_6698037insGTA	GRCh37
NC_000019.8:g.6649036_6649037insGTA	NCBI36
NG_009557.1:g.27628_27629insCTA , LRG_27:g.27628_27629insCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-230_789-229insCTA
ENST00000695652.1:c.2318-230_2318-229insCTA	ENSP00000512083.1:n.2318-230_2318-229insCTA
ENST00000695653.1:c.350-230_350-229insCTA	ENSP00000512084.1:n.350-230_350-229insCTA
ENST00000695654.1:c.1565-230_1565-229insCTA	ENSP00000512085.1:n.1565-230_1565-229insCTA
ENST00000695655.1:c.1382-230_1382-229insCTA	ENSP00000512086.1:n.1382-230_1382-229insCTA
ENST00000695692.1:n.1805-230_1805-229insCTA
ENST00000245907.11:c.2441-230_2441-229insCTA MANE Select	ENSP00000245907.4:n.2441-230_2441-229insCTA
ENST00000245907.10:c.2441-230_2441-229insCTA	ENSP00000245907.4:n.2441-230_2441-229insCTA
ENST00000602053.1:n.489-230_489-229insCTA
NM_000064.3:c.2441-230_2441-229insCTA	NP_000055.2:n.2441-230_2441-229insCTA
NM_000064.4:c.2441-230_2441-229insCTA MANE Select	NP_000055.2:n.2441-230_2441-229insCTA