Canonical Allele Identifier: CA2320568004

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713598_6713599delinsGC , CM000681.2:g.6713598_6713599delinsGC	GRCh38
NC_000019.9:g.6713609_6713610delinsGC , CM000681.1:g.6713609_6713610delinsGC	GRCh37
NC_000019.8:g.6664609_6664610delinsGC	NCBI36
NG_009557.1:g.12053_12054delinsGC , LRG_27:g.12053_12054delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-90_651-89delinsGC	ENSP00000512083.1:n.651-90_651-89delinsGC
ENST00000695692.1:n.8_9delinsGC
ENST00000245907.11:c.774-90_774-89delinsGC MANE Select	ENSP00000245907.4:n.774-90_774-89delinsGC
ENST00000245907.10:c.774-90_774-89delinsGC	ENSP00000245907.4:n.774-90_774-89delinsGC
ENST00000595577.1:n.278-90_278-89delinsGC
ENST00000597442.5:n.24-90_24-89delinsGC
NM_000064.3:c.774-90_774-89delinsGC	NP_000055.2:n.774-90_774-89delinsGC
NM_000064.4:c.774-90_774-89delinsGC MANE Select	NP_000055.2:n.774-90_774-89delinsGC