Canonical Allele Identifier: CA2587873212

Gene: C3

Linked Data

• gnomAD v4: 19-6685171-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685171_6685172insT , CM000681.2:g.6685171_6685172insT	GRCh38
NC_000019.9:g.6685182_6685183insT , CM000681.1:g.6685182_6685183insT	GRCh37
NC_000019.8:g.6636182_6636183insT	NCBI36
NG_009557.1:g.40480_40481insA , LRG_27:g.40480_40481insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2159-26_2159-25insA
ENST00000695653.1:c.1720-26_1720-25insA	ENSP00000512084.1:n.1720-26_1720-25insA
ENST00000695654.1:c.2836-26_2836-25insA	ENSP00000512085.1:n.2836-26_2836-25insA
ENST00000245907.11:c.3811-26_3811-25insA MANE Select	ENSP00000245907.4:n.3811-26_3811-25insA
ENST00000245907.10:c.3811-26_3811-25insA	ENSP00000245907.4:n.3811-26_3811-25insA
ENST00000596238.1:n.254-26_254-25insA
ENST00000601008.1:c.241+1574_241+1575insA	ENSP00000471384.1:n.241+1574_241+1575insA
NM_000064.3:c.3811-26_3811-25insA	NP_000055.2:n.3811-26_3811-25insA
NM_000064.4:c.3811-26_3811-25insA MANE Select	NP_000055.2:n.3811-26_3811-25insA