Canonical Allele Identifier: CA2320553467

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686203T= , CM000681.2:g.6686203T=	GRCh38
NC_000019.9:g.6686214T= , CM000681.1:g.6686214T=	GRCh37
NC_000019.8:g.6637214T=	NCBI36
NG_009557.1:g.39449A= , LRG_27:g.39449A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2079A=
ENST00000695652.1:c.3608A=	ENSP00000512083.1:p.Lys1203=
ENST00000695653.1:c.1640A=	ENSP00000512084.1:p.Lys547=
ENST00000695654.1:c.2756A=	ENSP00000512085.1:p.Lys919=
ENST00000695655.1:c.2672A=	ENSP00000512086.1:n.2672A=
ENST00000695692.1:n.3095A=
ENST00000245907.11:c.3731A= MANE Select	ENSP00000245907.4:p.Lys1244=
ENST00000245907.10:c.3731A=	ENSP00000245907.4:p.Lys1244=
ENST00000596238.1:n.174A=
ENST00000601008.1:c.241+543A=	ENSP00000471384.1:n.241+543A=
NM_000064.3:c.3731A=	NP_000055.2:p.Lys1244=
NM_000064.4:c.3731A= MANE Select	NP_000055.2:p.Lys1244=