Canonical Allele Identifier: CA2587878447
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713654_6713663del , CM000681.2:g.6713654_6713663del GRCh38
NC_000019.9:g.6713665_6713674del , CM000681.1:g.6713665_6713674del GRCh37
NC_000019.8:g.6664665_6664674del NCBI36
NG_009557.1:g.11989_11998del , LRG_27:g.11989_11998del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-154_651-145del ENSP00000512083.1:n.651-154_651-145del
ENST00000245907.11:c.774-154_774-145del MANE Select ENSP00000245907.4:n.774-154_774-145del
ENST00000245907.10:c.774-154_774-145del ENSP00000245907.4:n.774-154_774-145del
ENST00000595577.1:n.278-154_278-145del
ENST00000597442.5:n.23+103_23+112del
NM_000064.3:c.774-154_774-145del NP_000055.2:n.774-154_774-145del
NM_000064.4:c.774-154_774-145del MANE Select NP_000055.2:n.774-154_774-145del