Canonical Allele Identifier: CA2813446705

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713674_6713675insGA , CM000681.2:g.6713674_6713675insGA	GRCh38
NC_000019.9:g.6713685_6713686insGA , CM000681.1:g.6713685_6713686insGA	GRCh37
NC_000019.8:g.6664685_6664686insGA	NCBI36
NG_009557.1:g.11977_11978insTC , LRG_27:g.11977_11978insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-166_651-165insTC	ENSP00000512083.1:n.651-166_651-165insTC
ENST00000245907.11:c.774-166_774-165insTC MANE Select	ENSP00000245907.4:n.774-166_774-165insTC
ENST00000245907.10:c.774-166_774-165insTC	ENSP00000245907.4:n.774-166_774-165insTC
ENST00000595577.1:n.278-166_278-165insTC
ENST00000597442.5:n.23+91_23+92insTC
NM_000064.3:c.774-166_774-165insTC	NP_000055.2:n.774-166_774-165insTC
NM_000064.4:c.774-166_774-165insTC MANE Select	NP_000055.2:n.774-166_774-165insTC