Canonical Allele Identifier: CA2587871644

Gene: C3

Linked Data

• gnomAD v4: 19-6678999-T-TCA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679007_6679008dup , CM000681.2:g.6679007_6679008dup	GRCh38
NC_000019.9:g.6679018_6679019dup , CM000681.1:g.6679018_6679019dup	GRCh37
NC_000019.8:g.6630018_6630019dup	NCBI36
NG_009557.1:g.46651_46652dup , LRG_27:g.46651_46652dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2978+124_2978+125dup
ENST00000695653.1:c.2539+124_2539+125dup	ENSP00000512084.1:n.2539+124_2539+125dup
ENST00000695654.1:c.3655+124_3655+125dup	ENSP00000512085.1:n.3655+124_3655+125dup
ENST00000695689.1:c.601+124_601+125dup	ENSP00000512101.1:n.601+124_601+125dup
ENST00000695690.1:n.1695+124_1695+125dup
ENST00000695691.1:n.1491+124_1491+125dup
ENST00000245907.11:c.4630+124_4630+125dup MANE Select	ENSP00000245907.4:n.4630+124_4630+125dup
ENST00000245907.10:c.4630+124_4630+125dup	ENSP00000245907.4:n.4630+124_4630+125dup
ENST00000599668.1:n.250+124_250+125dup
ENST00000599899.5:n.1589+124_1589+125dup
ENST00000601008.1:c.242-1043_242-1042dup	ENSP00000471384.1:n.242-1043_242-1042dup
ENST00000602229.1:c.77+124_77+125dup
NM_000064.3:c.4630+124_4630+125dup	NP_000055.2:n.4630+124_4630+125dup
NM_000064.4:c.4630+124_4630+125dup MANE Select	NP_000055.2:n.4630+124_4630+125dup