Canonical Allele Identifier: CA2320551587

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682074_6682075delinsCT , CM000681.2:g.6682074_6682075delinsCT	GRCh38
NC_000019.9:g.6682085_6682086delinsCT , CM000681.1:g.6682085_6682086delinsCT	GRCh37
NC_000019.8:g.6633085_6633086delinsCT	NCBI36
NG_009557.1:g.43577_43578delinsAG , LRG_27:g.43577_43578delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2609-45_2609-44delinsAG
ENST00000695653.1:c.2170-45_2170-44delinsAG	ENSP00000512084.1:n.2170-45_2170-44delinsAG
ENST00000695654.1:c.3286-45_3286-44delinsAG	ENSP00000512085.1:n.3286-45_3286-44delinsAG
ENST00000695689.1:c.232-45_232-44delinsAG	ENSP00000512101.1:n.232-45_232-44delinsAG
ENST00000695690.1:n.452-45_452-44delinsAG
ENST00000695691.1:n.452-45_452-44delinsAG
ENST00000245907.11:c.4261-45_4261-44delinsAG MANE Select	ENSP00000245907.4:n.4261-45_4261-44delinsAG
ENST00000245907.10:c.4261-45_4261-44delinsAG	ENSP00000245907.4:n.4261-45_4261-44delinsAG
ENST00000596548.1:c.382-45_382-44delinsAG	ENSP00000469744.1:n.382-45_382-44delinsAG
ENST00000599899.5:n.1220-45_1220-44delinsAG
ENST00000601008.1:c.242-4117_242-4116delinsAG	ENSP00000471384.1:n.242-4117_242-4116delinsAG
NM_000064.3:c.4261-45_4261-44delinsAG	NP_000055.2:n.4261-45_4261-44delinsAG
NM_000064.4:c.4261-45_4261-44delinsAG MANE Select	NP_000055.2:n.4261-45_4261-44delinsAG