Canonical Allele Identifier: CA2813446709

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713746_6713863del , CM000681.2:g.6713746_6713863del	GRCh38
NC_000019.9:g.6713757_6713874del , CM000681.1:g.6713757_6713874del	GRCh37
NC_000019.8:g.6664757_6664874del	NCBI36
NG_009557.1:g.11811_11928del , LRG_27:g.11811_11928del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.650+151_651-215del	ENSP00000512083.1:n.650+151_651-215del
ENST00000245907.11:c.773+151_774-215del MANE Select	ENSP00000245907.4:n.773+151_774-215del
ENST00000245907.10:c.773+151_774-215del	ENSP00000245907.4:n.773+151_774-215del
ENST00000595577.1:n.277+151_278-215del
NM_000064.3:c.773+151_774-215del	NP_000055.2:n.773+151_774-215del
NM_000064.4:c.773+151_774-215del MANE Select	NP_000055.2:n.773+151_774-215del