Canonical Allele Identifier: CA2320567999

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713578_6713579delinsTG , CM000681.2:g.6713578_6713579delinsTG	GRCh38
NC_000019.9:g.6713589_6713590delinsTG , CM000681.1:g.6713589_6713590delinsTG	GRCh37
NC_000019.8:g.6664589_6664590delinsTG	NCBI36
NG_009557.1:g.12073_12074delinsCA , LRG_27:g.12073_12074delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-70_651-69delinsCA	ENSP00000512083.1:n.651-70_651-69delinsCA
ENST00000695692.1:n.28_29delinsCA
ENST00000245907.11:c.774-70_774-69delinsCA MANE Select	ENSP00000245907.4:n.774-70_774-69delinsCA
ENST00000245907.10:c.774-70_774-69delinsCA	ENSP00000245907.4:n.774-70_774-69delinsCA
ENST00000595577.1:n.278-70_278-69delinsCA
ENST00000597442.5:n.24-70_24-69delinsCA
NM_000064.3:c.774-70_774-69delinsCA	NP_000055.2:n.774-70_774-69delinsCA
NM_000064.4:c.774-70_774-69delinsCA MANE Select	NP_000055.2:n.774-70_774-69delinsCA