Canonical Allele Identifier: CA2320568076

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713682_6713683delinsCT , CM000681.2:g.6713682_6713683delinsCT	GRCh38
NC_000019.9:g.6713693_6713694delinsCT , CM000681.1:g.6713693_6713694delinsCT	GRCh37
NC_000019.8:g.6664693_6664694delinsCT	NCBI36
NG_009557.1:g.11969_11970delinsAG , LRG_27:g.11969_11970delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-174_651-173delinsAG	ENSP00000512083.1:n.651-174_651-173delinsAG
ENST00000245907.11:c.774-174_774-173delinsAG MANE Select	ENSP00000245907.4:n.774-174_774-173delinsAG
ENST00000245907.10:c.774-174_774-173delinsAG	ENSP00000245907.4:n.774-174_774-173delinsAG
ENST00000595577.1:n.278-174_278-173delinsAG
ENST00000597442.5:n.23+83_23+84delinsAG
NM_000064.3:c.774-174_774-173delinsAG	NP_000055.2:n.774-174_774-173delinsAG
NM_000064.4:c.774-174_774-173delinsAG MANE Select	NP_000055.2:n.774-174_774-173delinsAG