Canonical Allele Identifier: CA2320551499

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681880_6681881delinsCA , CM000681.2:g.6681880_6681881delinsCA	GRCh38
NC_000019.9:g.6681891_6681892delinsCA , CM000681.1:g.6681891_6681892delinsCA	GRCh37
NC_000019.8:g.6632891_6632892delinsCA	NCBI36
NG_009557.1:g.43771_43772delinsTG , LRG_27:g.43771_43772delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2698+60_2698+61delinsTG
ENST00000695653.1:c.2259+60_2259+61delinsTG	ENSP00000512084.1:n.2259+60_2259+61delinsTG
ENST00000695654.1:c.3375+60_3375+61delinsTG	ENSP00000512085.1:n.3375+60_3375+61delinsTG
ENST00000695689.1:c.321+60_321+61delinsTG	ENSP00000512101.1:n.321+60_321+61delinsTG
ENST00000695690.1:n.601_602delinsTG
ENST00000695691.1:n.601_602delinsTG
ENST00000245907.11:c.4350+60_4350+61delinsTG MANE Select	ENSP00000245907.4:n.4350+60_4350+61delinsTG
ENST00000245907.10:c.4350+60_4350+61delinsTG	ENSP00000245907.4:n.4350+60_4350+61delinsTG
ENST00000596548.1:c.471+60_471+61delinsTG	ENSP00000469744.1:n.471+60_471+61delinsTG
ENST00000599899.5:n.1309+60_1309+61delinsTG
ENST00000601008.1:c.242-3923_242-3922delinsTG	ENSP00000471384.1:n.242-3923_242-3922delinsTG
NM_000064.3:c.4350+60_4350+61delinsTG	NP_000055.2:n.4350+60_4350+61delinsTG
NM_000064.4:c.4350+60_4350+61delinsTG MANE Select	NP_000055.2:n.4350+60_4350+61delinsTG