Canonical Allele Identifier: CA2320568023
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713629_6713700delinsCCCCACCTCCAGCCCCTCACCTGGCCCCACCCCCAGCCCCCCACCTTGCCCCACTCCCACCCCCCACATGGT , CM000681.2:g.6713629_6713700delinsCCCCACCTCCAGCCCCTCACCTGGCCCCACCCCCAGCCCCCCACCTTGCCCCACTCCCACCCCCCACATGGT GRCh38
NC_000019.9:g.6713640_6713711delinsCCCCACCTCCAGCCCCTCACCTGGCCCCACCCCCAGCCCCCCACCTTGCCCCACTCCCACCCCCCACATGGT , CM000681.1:g.6713640_6713711delinsCCCCACCTCCAGCCCCTCACCTGGCCCCACCCCCAGCCCCCCACCTTGCCCCACTCCCACCCCCCACATGGT GRCh37
NC_000019.8:g.6664640_6664711delinsCCCCACCTCCAGCCCCTCACCTGGCCCCACCCCCAGCCCCCCACCTTGCCCCACTCCCACCCCCCACATGGT NCBI36
NG_009557.1:g.11952_12023delinsACCATGTGGGGGGTGGGAGTGGGGCAAGGTGGGGGGCTGGGGGTGGGGCCAGGTGAGGGGCTGGAGGTGGGG , LRG_27:g.11952_12023delinsACCATGTGGGGGGTGGGAGTGGGGCAAGGTGGGGGGCTGGGGGTGGGGCCAGGTGAGGGGCTGGAGGTGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-191_651-120delinsACCATGTGGGGGGTGGGAGTGGGGCAAGGTGGGGGGCTGGGGGTGGGGCCAGGTGAGGGGCTGGAGGTGGGG ENSP00000512083.1:n.651-191_651-120delinsACCATGTGGGGGGTGGGAGT...
ENST00000245907.11:c.774-191_774-120delinsACCATGTGGGGGGTGGGAGTGGGGCAAGGTGGGGGGCTGGGGGTGGGGCCAGGTGAGGGGCTGGAGGTGGGG MANE Select ENSP00000245907.4:n.774-191_774-120delinsACCATGTGGGGGGTGGGAGT...
ENST00000245907.10:c.774-191_774-120delinsACCATGTGGGGGGTGGGAGTGGGGCAAGGTGGGGGGCTGGGGGTGGGGCCAGGTGAGGGGCTGGAGGTGGGG ENSP00000245907.4:n.774-191_774-120delinsACCATGTGGGGGGTGGGAGT...
ENST00000595577.1:n.278-191_278-120delinsACCATGTGGGGGGTGGGAGTGGGGCAAGGTGGGGGGCTGGGGGTGGGGCCAGGTGAGGGGCTGGAGGTGGGG
ENST00000597442.5:n.23+66_24-120delinsACCATGTGGGGGGTGGGAGTGGGGCAAGGTGGGGGGCTGGGGGTGGGGCCAGGTGAGGGGCTGGAGGTGGGG
NM_000064.3:c.774-191_774-120delinsACCATGTGGGGGGTGGGAGTGGGGCAAGGTGGGGGGCTGGGGGTGGGGCCAGGTGAGGGGCTGGAGGTGGGG NP_000055.2:n.774-191_774-120delinsACCATGTGGGGGGTGGGAGTGGGGCA...
NM_000064.4:c.774-191_774-120delinsACCATGTGGGGGGTGGGAGTGGGGCAAGGTGGGGGGCTGGGGGTGGGGCCAGGTGAGGGGCTGGAGGTGGGG MANE Select NP_000055.2:n.774-191_774-120delinsACCATGTGGGGGGTGGGAGTGGGGCA...