Canonical Allele Identifier: CA2320551689

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682299_6682300delinsAG , CM000681.2:g.6682299_6682300delinsAG	GRCh38
NC_000019.9:g.6682310_6682311delinsAG , CM000681.1:g.6682310_6682311delinsAG	GRCh37
NC_000019.8:g.6633310_6633311delinsAG	NCBI36
NG_009557.1:g.43352_43353delinsCT , LRG_27:g.43352_43353delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2521-71_2521-70delinsCT
ENST00000695653.1:c.2082-71_2082-70delinsCT	ENSP00000512084.1:n.2082-71_2082-70delinsCT
ENST00000695654.1:c.3198-71_3198-70delinsCT	ENSP00000512085.1:n.3198-71_3198-70delinsCT
ENST00000695689.1:c.144-71_144-70delinsCT	ENSP00000512101.1:n.144-71_144-70delinsCT
ENST00000695690.1:n.364-71_364-70delinsCT
ENST00000695691.1:n.364-71_364-70delinsCT
ENST00000245907.11:c.4173-71_4173-70delinsCT MANE Select	ENSP00000245907.4:n.4173-71_4173-70delinsCT
ENST00000245907.10:c.4173-71_4173-70delinsCT	ENSP00000245907.4:n.4173-71_4173-70delinsCT
ENST00000596548.1:c.294-71_294-70delinsCT	ENSP00000469744.1:n.294-71_294-70delinsCT
ENST00000599899.5:n.1061_1062delinsCT
ENST00000601008.1:c.242-4342_242-4341delinsCT	ENSP00000471384.1:n.242-4342_242-4341delinsCT
NM_000064.3:c.4173-71_4173-70delinsCT	NP_000055.2:n.4173-71_4173-70delinsCT
NM_000064.4:c.4173-71_4173-70delinsCT MANE Select	NP_000055.2:n.4173-71_4173-70delinsCT