Canonical Allele Identifier: CA2320555655

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6690448_6690449delinsGC , CM000681.2:g.6690448_6690449delinsGC	GRCh38
NC_000019.9:g.6690459_6690460delinsGC , CM000681.1:g.6690459_6690460delinsGC	GRCh37
NC_000019.8:g.6641459_6641460delinsGC	NCBI36
NG_009557.1:g.35203_35204delinsGC , LRG_27:g.35203_35204delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1837+180_1837+181delinsGC
ENST00000695652.1:c.3366+180_3366+181delinsGC	ENSP00000512083.1:n.3366+180_3366+181delinsGC
ENST00000695653.1:c.1398+180_1398+181delinsGC	ENSP00000512084.1:n.1398+180_1398+181delinsGC
ENST00000695654.1:c.2514+2475_2514+2476delinsGC	ENSP00000512085.1:n.2514+2475_2514+2476delinsGC
ENST00000695655.1:c.2430+180_2430+181delinsGC	ENSP00000512086.1:n.2430+180_2430+181delinsGC
ENST00000695692.1:n.2853+180_2853+181delinsGC
ENST00000245907.11:c.3489+180_3489+181delinsGC MANE Select	ENSP00000245907.4:n.3489+180_3489+181delinsGC
ENST00000245907.10:c.3489+180_3489+181delinsGC	ENSP00000245907.4:n.3489+180_3489+181delinsGC
ENST00000598805.2:n.259+180_259+181delinsGC
ENST00000601008.1:c.84+180_84+181delinsGC	ENSP00000471384.1:n.84+180_84+181delinsGC
NM_000064.3:c.3489+180_3489+181delinsGC	NP_000055.2:n.3489+180_3489+181delinsGC
NM_000064.4:c.3489+180_3489+181delinsGC MANE Select	NP_000055.2:n.3489+180_3489+181delinsGC