Canonical Allele Identifier: CA2813446560

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710025_6710026insAGGGAGAGAGAGGGAGAGTGGG , CM000681.2:g.6710025_6710026insAGGGAGAGAGAGGGAGAGTGGG	GRCh38
NC_000019.9:g.6710036_6710037insAGGGAGAGAGAGGGAGAGTGGG , CM000681.1:g.6710036_6710037insAGGGAGAGAGAGGGAGAGTGGG	GRCh37
NC_000019.8:g.6661036_6661037insAGGGAGAGAGAGGGAGAGTGGG	NCBI36
NG_009557.1:g.15629_15630insACTCTCCCTCTCTCTCCCTCCC , LRG_27:g.15629_15630insACTCTCCCTCTCTCTCCCTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-181_1564-180insACTCTCCCTCTCTCTCCCTCCC	ENSP00000512083.1:n.1564-181_1564-180insACTCTCCCTCTCTCTCCCTCC...
ENST00000695654.1:c.811-181_811-180insACTCTCCCTCTCTCTCCCTCCC	ENSP00000512085.1:n.811-181_811-180insACTCTCCCTCTCTCTCCCTCCC
ENST00000695655.1:c.592-145_592-144insACTCTCCCTCTCTCTCCCTCCC	ENSP00000512086.1:n.592-145_592-144insACTCTCCCTCTCTCTCCCTCCC
ENST00000695692.1:n.1051-181_1051-180insACTCTCCCTCTCTCTCCCTCCC
ENST00000245907.11:c.1687-181_1687-180insACTCTCCCTCTCTCTCCCTCCC MANE Select	ENSP00000245907.4:n.1687-181_1687-180insACTCTCCCTCTCTCTCCCTCC...
ENST00000245907.10:c.1687-181_1687-180insACTCTCCCTCTCTCTCCCTCCC	ENSP00000245907.4:n.1687-181_1687-180insACTCTCCCTCTCTCTCCCTCC...
ENST00000600763.1:n.320-181_320-180insACTCTCCCTCTCTCTCCCTCCC
NM_000064.3:c.1687-181_1687-180insACTCTCCCTCTCTCTCCCTCCC	NP_000055.2:n.1687-181_1687-180insACTCTCCCTCTCTCTCCCTCCC
NM_000064.4:c.1687-181_1687-180insACTCTCCCTCTCTCTCCCTCCC MANE Select	NP_000055.2:n.1687-181_1687-180insACTCTCCCTCTCTCTCCCTCCC