Canonical Allele Identifier: CA2735579647

Gene: C3

Linked Data

• dbSNP Id: rs2145396728

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685148_6685149insGGGT , CM000681.2:g.6685148_6685149insGGGT	GRCh38
NC_000019.9:g.6685159_6685160insGGGT , CM000681.1:g.6685159_6685160insGGGT	GRCh37
NC_000019.8:g.6636159_6636160insGGGT	NCBI36
NG_009557.1:g.40504_40505insCCCA , LRG_27:g.40504_40505insCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2159-2_2159-1insCCCA
ENST00000695653.1:c.1720-2_1720-1insCCCA	ENSP00000512084.1:n.1720-2_1720-1insCCCA
ENST00000695654.1:c.2836-2_2836-1insCCCA	ENSP00000512085.1:n.2836-2_2836-1insCCCA
ENST00000245907.11:c.3811-2_3811-1insCCCA MANE Select	ENSP00000245907.4:n.3811-2_3811-1insCCCA
ENST00000245907.10:c.3811-2_3811-1insCCCA	ENSP00000245907.4:n.3811-2_3811-1insCCCA
ENST00000596238.1:n.254-2_254-1insCCCA
ENST00000601008.1:c.241+1598_241+1599insCCCA	ENSP00000471384.1:n.241+1598_241+1599insCCCA
NM_000064.3:c.3811-2_3811-1insCCCA	NP_000055.2:n.3811-2_3811-1insCCCA
NM_000064.4:c.3811-2_3811-1insCCCA MANE Select	NP_000055.2:n.3811-2_3811-1insCCCA