Canonical Allele Identifier: CA2320552831

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6684942_6684943delinsAG , CM000681.2:g.6684942_6684943delinsAG	GRCh38
NC_000019.9:g.6684953_6684954delinsAG , CM000681.1:g.6684953_6684954delinsAG	GRCh37
NC_000019.8:g.6635953_6635954delinsAG	NCBI36
NG_009557.1:g.40709_40710delinsCT , LRG_27:g.40709_40710delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2317+45_2317+46delinsCT
ENST00000695653.1:c.1878+45_1878+46delinsCT	ENSP00000512084.1:n.1878+45_1878+46delinsCT
ENST00000695654.1:c.2994+45_2994+46delinsCT	ENSP00000512085.1:n.2994+45_2994+46delinsCT
ENST00000695690.1:n.160+45_160+46delinsCT
ENST00000695691.1:n.160+45_160+46delinsCT
ENST00000245907.11:c.3969+45_3969+46delinsCT MANE Select	ENSP00000245907.4:n.3969+45_3969+46delinsCT
ENST00000245907.10:c.3969+45_3969+46delinsCT	ENSP00000245907.4:n.3969+45_3969+46delinsCT
ENST00000596238.1:n.412+45_412+46delinsCT
ENST00000596548.1:c.51+45_51+46delinsCT	ENSP00000469744.1:n.51+45_51+46delinsCT
ENST00000601008.1:c.241+1803_241+1804delinsCT	ENSP00000471384.1:n.241+1803_241+1804delinsCT
NM_000064.3:c.3969+45_3969+46delinsCT	NP_000055.2:n.3969+45_3969+46delinsCT
NM_000064.4:c.3969+45_3969+46delinsCT MANE Select	NP_000055.2:n.3969+45_3969+46delinsCT