Canonical Allele Identifier: CA2813446696

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713326_6713327insTT , CM000681.2:g.6713326_6713327insTT	GRCh38
NC_000019.9:g.6713337_6713338insTT , CM000681.1:g.6713337_6713338insTT	GRCh37
NC_000019.8:g.6664337_6664338insTT	NCBI36
NG_009557.1:g.12325_12326insAA , LRG_27:g.12325_12326insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.754-12_754-11insAA	ENSP00000512083.1:n.754-12_754-11insAA
ENST00000695692.1:n.201-12_201-11insAA
ENST00000245907.11:c.877-12_877-11insAA MANE Select	ENSP00000245907.4:n.877-12_877-11insAA
ENST00000245907.10:c.877-12_877-11insAA	ENSP00000245907.4:n.877-12_877-11insAA
ENST00000595577.1:n.381-12_381-11insAA
ENST00000597442.5:n.127-12_127-11insAA
NM_000064.3:c.877-12_877-11insAA	NP_000055.2:n.877-12_877-11insAA
NM_000064.4:c.877-12_877-11insAA MANE Select	NP_000055.2:n.877-12_877-11insAA