Canonical Allele Identifier: CA2320568054

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713663_6713664delinsAG , CM000681.2:g.6713663_6713664delinsAG	GRCh38
NC_000019.9:g.6713674_6713675delinsAG , CM000681.1:g.6713674_6713675delinsAG	GRCh37
NC_000019.8:g.6664674_6664675delinsAG	NCBI36
NG_009557.1:g.11988_11989delinsCT , LRG_27:g.11988_11989delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-155_651-154delinsCT	ENSP00000512083.1:n.651-155_651-154delinsCT
ENST00000245907.11:c.774-155_774-154delinsCT MANE Select	ENSP00000245907.4:n.774-155_774-154delinsCT
ENST00000245907.10:c.774-155_774-154delinsCT	ENSP00000245907.4:n.774-155_774-154delinsCT
ENST00000595577.1:n.278-155_278-154delinsCT
ENST00000597442.5:n.23+102_23+103delinsCT
NM_000064.3:c.774-155_774-154delinsCT	NP_000055.2:n.774-155_774-154delinsCT
NM_000064.4:c.774-155_774-154delinsCT MANE Select	NP_000055.2:n.774-155_774-154delinsCT