Canonical Allele Identifier: CA2576592411

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713602_6713603del , CM000681.2:g.6713602_6713603del	GRCh38
NC_000019.9:g.6713613_6713614del , CM000681.1:g.6713613_6713614del	GRCh37
NC_000019.8:g.6664613_6664614del	NCBI36
NG_009557.1:g.12052_12053del , LRG_27:g.12052_12053del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-91_651-90del	ENSP00000512083.1:n.651-91_651-90del
ENST00000695692.1:n.7_8del
ENST00000245907.11:c.774-91_774-90del MANE Select	ENSP00000245907.4:n.774-91_774-90del
ENST00000245907.10:c.774-91_774-90del	ENSP00000245907.4:n.774-91_774-90del
ENST00000595577.1:n.278-91_278-90del
ENST00000597442.5:n.24-91_24-90del
NM_000064.3:c.774-91_774-90del	NP_000055.2:n.774-91_774-90del
NM_000064.4:c.774-91_774-90del MANE Select	NP_000055.2:n.774-91_774-90del