Canonical Allele Identifier: CA2320567886

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713360_6713361delinsGT , CM000681.2:g.6713360_6713361delinsGT	GRCh38
NC_000019.9:g.6713371_6713372delinsGT , CM000681.1:g.6713371_6713372delinsGT	GRCh37
NC_000019.8:g.6664371_6664372delinsGT	NCBI36
NG_009557.1:g.12291_12292delinsAC , LRG_27:g.12291_12292delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.754-46_754-45delinsAC	ENSP00000512083.1:n.754-46_754-45delinsAC
ENST00000695692.1:n.201-46_201-45delinsAC
ENST00000245907.11:c.877-46_877-45delinsAC MANE Select	ENSP00000245907.4:n.877-46_877-45delinsAC
ENST00000245907.10:c.877-46_877-45delinsAC	ENSP00000245907.4:n.877-46_877-45delinsAC
ENST00000595577.1:n.381-46_381-45delinsAC
ENST00000597442.5:n.127-46_127-45delinsAC
NM_000064.3:c.877-46_877-45delinsAC	NP_000055.2:n.877-46_877-45delinsAC
NM_000064.4:c.877-46_877-45delinsAC MANE Select	NP_000055.2:n.877-46_877-45delinsAC