Canonical Allele Identifier: CA2320567992
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713573_6713576delinsTCTC , CM000681.2:g.6713573_6713576delinsTCTC GRCh38
NC_000019.9:g.6713584_6713587delinsTCTC , CM000681.1:g.6713584_6713587delinsTCTC GRCh37
NC_000019.8:g.6664584_6664587delinsTCTC NCBI36
NG_009557.1:g.12076_12079delinsGAGA , LRG_27:g.12076_12079delinsGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-67_651-64delinsGAGA ENSP00000512083.1:n.651-67_651-64delinsGAGA
ENST00000695692.1:n.31_34delinsGAGA
ENST00000245907.11:c.774-67_774-64delinsGAGA MANE Select ENSP00000245907.4:n.774-67_774-64delinsGAGA
ENST00000245907.10:c.774-67_774-64delinsGAGA ENSP00000245907.4:n.774-67_774-64delinsGAGA
ENST00000595577.1:n.278-67_278-64delinsGAGA
ENST00000597442.5:n.24-67_24-64delinsGAGA
NM_000064.3:c.774-67_774-64delinsGAGA NP_000055.2:n.774-67_774-64delinsGAGA
NM_000064.4:c.774-67_774-64delinsGAGA MANE Select NP_000055.2:n.774-67_774-64delinsGAGA