Canonical Allele Identifier: CA2545172215

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710025_6710026insAGGGAGAGAGAGAGAGAGGG , CM000681.2:g.6710025_6710026insAGGGAGAGAGAGAGAGAGGG	GRCh38
NC_000019.9:g.6710036_6710037insAGGGAGAGAGAGAGAGAGGG , CM000681.1:g.6710036_6710037insAGGGAGAGAGAGAGAGAGGG	GRCh37
NC_000019.8:g.6661036_6661037insAGGGAGAGAGAGAGAGAGGG	NCBI36
NG_009557.1:g.15635_15636insTCTCTCTCCCTCCCTCTCTC , LRG_27:g.15635_15636insTCTCTCTCCCTCCCTCTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-175_1564-174insTCTCTCTCCCTCCCTCTCTC	ENSP00000512083.1:n.1564-175_1564-174insTCTCTCTCCCTCCCTCTCTC
ENST00000695654.1:c.811-175_811-174insTCTCTCTCCCTCCCTCTCTC	ENSP00000512085.1:n.811-175_811-174insTCTCTCTCCCTCCCTCTCTC
ENST00000695655.1:c.592-139_592-138insTCTCTCTCCCTCCCTCTCTC	ENSP00000512086.1:n.592-139_592-138insTCTCTCTCCCTCCCTCTCTC
ENST00000695692.1:n.1051-175_1051-174insTCTCTCTCCCTCCCTCTCTC
ENST00000245907.11:c.1687-175_1687-174insTCTCTCTCCCTCCCTCTCTC MANE Select	ENSP00000245907.4:n.1687-175_1687-174insTCTCTCTCCCTCCCTCTCTC
ENST00000245907.10:c.1687-175_1687-174insTCTCTCTCCCTCCCTCTCTC	ENSP00000245907.4:n.1687-175_1687-174insTCTCTCTCCCTCCCTCTCTC
ENST00000600763.1:n.320-175_320-174insTCTCTCTCCCTCCCTCTCTC
NM_000064.3:c.1687-175_1687-174insTCTCTCTCCCTCCCTCTCTC	NP_000055.2:n.1687-175_1687-174insTCTCTCTCCCTCCCTCTCTC
NM_000064.4:c.1687-175_1687-174insTCTCTCTCCCTCCCTCTCTC MANE Select	NP_000055.2:n.1687-175_1687-174insTCTCTCTCCCTCCCTCTCTC