Canonical Allele Identifier: CA2832508836

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713816_6713818del , CM000681.2:g.6713816_6713818del	GRCh38
NC_000019.9:g.6713827_6713829del , CM000681.1:g.6713827_6713829del	GRCh37
NC_000019.8:g.6664827_6664829del	NCBI36
NG_009557.1:g.11834_11836del , LRG_27:g.11834_11836del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.650+174_650+176del	ENSP00000512083.1:n.650+174_650+176del
ENST00000245907.11:c.773+174_773+176del MANE Select	ENSP00000245907.4:n.773+174_773+176del
ENST00000245907.10:c.773+174_773+176del	ENSP00000245907.4:n.773+174_773+176del
ENST00000595577.1:n.277+174_277+176del
NM_000064.3:c.773+174_773+176del	NP_000055.2:n.773+174_773+176del
NM_000064.4:c.773+174_773+176del MANE Select	NP_000055.2:n.773+174_773+176del