Canonical Allele Identifier: CA2320567969

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713540_6713541delinsCA , CM000681.2:g.6713540_6713541delinsCA	GRCh38
NC_000019.9:g.6713551_6713552delinsCA , CM000681.1:g.6713551_6713552delinsCA	GRCh37
NC_000019.8:g.6664551_6664552delinsCA	NCBI36
NG_009557.1:g.12111_12112delinsTG , LRG_27:g.12111_12112delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-32_651-31delinsTG	ENSP00000512083.1:n.651-32_651-31delinsTG
ENST00000695692.1:n.66_67delinsTG
ENST00000245907.11:c.774-32_774-31delinsTG MANE Select	ENSP00000245907.4:n.774-32_774-31delinsTG
ENST00000245907.10:c.774-32_774-31delinsTG	ENSP00000245907.4:n.774-32_774-31delinsTG
ENST00000595577.1:n.278-32_278-31delinsTG
ENST00000597442.5:n.24-32_24-31delinsTG
NM_000064.3:c.774-32_774-31delinsTG	NP_000055.2:n.774-32_774-31delinsTG
NM_000064.4:c.774-32_774-31delinsTG MANE Select	NP_000055.2:n.774-32_774-31delinsTG