Canonical Allele Identifier: CA2320566113

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710040_6710044delinsAAAGG , CM000681.2:g.6710040_6710044delinsAAAGG	GRCh38
NC_000019.9:g.6710051_6710055delinsAAAGG , CM000681.1:g.6710051_6710055delinsAAAGG	GRCh37
NC_000019.8:g.6661051_6661055delinsAAAGG	NCBI36
NG_009557.1:g.15608_15612delinsCCTTT , LRG_27:g.15608_15612delinsCCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-202_1564-198delinsCCTTT	ENSP00000512083.1:n.1564-202_1564-198delinsCCTTT
ENST00000695654.1:c.811-202_811-198delinsCCTTT	ENSP00000512085.1:n.811-202_811-198delinsCCTTT
ENST00000695655.1:c.592-166_592-162delinsCCTTT	ENSP00000512086.1:n.592-166_592-162delinsCCTTT
ENST00000695692.1:n.1051-202_1051-198delinsCCTTT
ENST00000245907.11:c.1687-202_1687-198delinsCCTTT MANE Select	ENSP00000245907.4:n.1687-202_1687-198delinsCCTTT
ENST00000245907.10:c.1687-202_1687-198delinsCCTTT	ENSP00000245907.4:n.1687-202_1687-198delinsCCTTT
ENST00000600763.1:n.320-202_320-198delinsCCTTT
NM_000064.3:c.1687-202_1687-198delinsCCTTT	NP_000055.2:n.1687-202_1687-198delinsCCTTT
NM_000064.4:c.1687-202_1687-198delinsCCTTT MANE Select	NP_000055.2:n.1687-202_1687-198delinsCCTTT