Canonical Allele Identifier: CA2320568677

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714640_6714641delinsTC , CM000681.2:g.6714640_6714641delinsTC	GRCh38
NC_000019.9:g.6714651_6714652delinsTC , CM000681.1:g.6714651_6714652delinsTC	GRCh37
NC_000019.8:g.6665651_6665652delinsTC	NCBI36
NG_009557.1:g.11011_11012delinsGA , LRG_27:g.11011_11012delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.382-195_382-194delinsGA	ENSP00000512083.1:n.382-195_382-194delinsGA
ENST00000245907.11:c.505-195_505-194delinsGA MANE Select	ENSP00000245907.4:n.505-195_505-194delinsGA
ENST00000245907.10:c.505-195_505-194delinsGA	ENSP00000245907.4:n.505-195_505-194delinsGA
NM_000064.3:c.505-195_505-194delinsGA	NP_000055.2:n.505-195_505-194delinsGA
NM_000064.4:c.505-195_505-194delinsGA MANE Select	NP_000055.2:n.505-195_505-194delinsGA