Canonical Allele Identifier: CA2570501789

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710037_6710038insGGAGAGAGGGCGGGAGAG , CM000681.2:g.6710037_6710038insGGAGAGAGGGCGGGAGAG	GRCh38
NC_000019.9:g.6710048_6710049insGGAGAGAGGGCGGGAGAG , CM000681.1:g.6710048_6710049insGGAGAGAGGGCGGGAGAG	GRCh37
NC_000019.8:g.6661048_6661049insGGAGAGAGGGCGGGAGAG	NCBI36
NG_009557.1:g.15619_15620insCCGCCCTCTCTCCCTCTC , LRG_27:g.15619_15620insCCGCCCTCTCTCCCTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-191_1564-190insCCGCCCTCTCTCCCTCTC	ENSP00000512083.1:n.1564-191_1564-190insCCGCCCTCTCTCCCTCTC
ENST00000695654.1:c.811-191_811-190insCCGCCCTCTCTCCCTCTC	ENSP00000512085.1:n.811-191_811-190insCCGCCCTCTCTCCCTCTC
ENST00000695655.1:c.592-155_592-154insCCGCCCTCTCTCCCTCTC	ENSP00000512086.1:n.592-155_592-154insCCGCCCTCTCTCCCTCTC
ENST00000695692.1:n.1051-191_1051-190insCCGCCCTCTCTCCCTCTC
ENST00000245907.11:c.1687-191_1687-190insCCGCCCTCTCTCCCTCTC MANE Select	ENSP00000245907.4:n.1687-191_1687-190insCCGCCCTCTCTCCCTCTC
ENST00000245907.10:c.1687-191_1687-190insCCGCCCTCTCTCCCTCTC	ENSP00000245907.4:n.1687-191_1687-190insCCGCCCTCTCTCCCTCTC
ENST00000600763.1:n.320-191_320-190insCCGCCCTCTCTCCCTCTC
NM_000064.3:c.1687-191_1687-190insCCGCCCTCTCTCCCTCTC	NP_000055.2:n.1687-191_1687-190insCCGCCCTCTCTCCCTCTC
NM_000064.4:c.1687-191_1687-190insCCGCCCTCTCTCCCTCTC MANE Select	NP_000055.2:n.1687-191_1687-190insCCGCCCTCTCTCCCTCTC