Canonical Allele Identifier: CA2813446724

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713854_6713925dup , CM000681.2:g.6713854_6713925dup	GRCh38
NC_000019.9:g.6713865_6713936dup , CM000681.1:g.6713865_6713936dup	GRCh37
NC_000019.8:g.6664865_6664936dup	NCBI36
NG_009557.1:g.11737_11808dup , LRG_27:g.11737_11808dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.650+77_650+148dup	ENSP00000512083.1:n.650+77_650+148dup
ENST00000245907.11:c.773+77_773+148dup MANE Select	ENSP00000245907.4:n.773+77_773+148dup
ENST00000245907.10:c.773+77_773+148dup	ENSP00000245907.4:n.773+77_773+148dup
ENST00000595577.1:n.277+77_277+148dup
NM_000064.3:c.773+77_773+148dup	NP_000055.2:n.773+77_773+148dup
NM_000064.4:c.773+77_773+148dup MANE Select	NP_000055.2:n.773+77_773+148dup