Canonical Allele Identifier: CA2320568438

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714141_6714142delinsTC , CM000681.2:g.6714141_6714142delinsTC	GRCh38
NC_000019.9:g.6714152_6714153delinsTC , CM000681.1:g.6714152_6714153delinsTC	GRCh37
NC_000019.8:g.6665152_6665153delinsTC	NCBI36
NG_009557.1:g.11510_11511delinsGA , LRG_27:g.11510_11511delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.559+24_559+25delinsGA	ENSP00000512083.1:n.559+24_559+25delinsGA
ENST00000245907.11:c.682+24_682+25delinsGA MANE Select	ENSP00000245907.4:n.682+24_682+25delinsGA
ENST00000245907.10:c.682+24_682+25delinsGA	ENSP00000245907.4:n.682+24_682+25delinsGA
ENST00000595577.1:n.186+24_186+25delinsGA
NM_000064.3:c.682+24_682+25delinsGA	NP_000055.2:n.682+24_682+25delinsGA
NM_000064.4:c.682+24_682+25delinsGA MANE Select	NP_000055.2:n.682+24_682+25delinsGA