Canonical Allele Identifier: CA2587873172

Gene: C3

Linked Data

• gnomAD v4: 19-6684898-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6684898_6684899insTT , CM000681.2:g.6684898_6684899insTT	GRCh38
NC_000019.9:g.6684909_6684910insTT , CM000681.1:g.6684909_6684910insTT	GRCh37
NC_000019.8:g.6635909_6635910insTT	NCBI36
NG_009557.1:g.40753_40754insAA , LRG_27:g.40753_40754insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2318-65_2318-64insAA
ENST00000695653.1:c.1879-65_1879-64insAA	ENSP00000512084.1:n.1879-65_1879-64insAA
ENST00000695654.1:c.2995-65_2995-64insAA	ENSP00000512085.1:n.2995-65_2995-64insAA
ENST00000695690.1:n.161-65_161-64insAA
ENST00000695691.1:n.161-65_161-64insAA
ENST00000245907.11:c.3970-65_3970-64insAA MANE Select	ENSP00000245907.4:n.3970-65_3970-64insAA
ENST00000245907.10:c.3970-65_3970-64insAA	ENSP00000245907.4:n.3970-65_3970-64insAA
ENST00000596238.1:n.413-65_413-64insAA
ENST00000596548.1:c.52-65_52-64insAA	ENSP00000469744.1:n.52-65_52-64insAA
ENST00000601008.1:c.241+1847_241+1848insAA	ENSP00000471384.1:n.241+1847_241+1848insAA
NM_000064.3:c.3970-65_3970-64insAA	NP_000055.2:n.3970-65_3970-64insAA
NM_000064.4:c.3970-65_3970-64insAA MANE Select	NP_000055.2:n.3970-65_3970-64insAA