Canonical Allele Identifier: CA2320552784

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6684847_6684849delinsAAG , CM000681.2:g.6684847_6684849delinsAAG	GRCh38
NC_000019.9:g.6684858_6684860delinsAAG , CM000681.1:g.6684858_6684860delinsAAG	GRCh37
NC_000019.8:g.6635858_6635860delinsAAG	NCBI36
NG_009557.1:g.40803_40805delinsCTT , LRG_27:g.40803_40805delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2318-15_2318-13delinsCTT
ENST00000695653.1:c.1879-15_1879-13delinsCTT	ENSP00000512084.1:n.1879-15_1879-13delinsCTT
ENST00000695654.1:c.2995-15_2995-13delinsCTT	ENSP00000512085.1:n.2995-15_2995-13delinsCTT
ENST00000695690.1:n.161-15_161-13delinsCTT
ENST00000695691.1:n.161-15_161-13delinsCTT
ENST00000245907.11:c.3970-15_3970-13delinsCTT MANE Select	ENSP00000245907.4:n.3970-15_3970-13delinsCTT
ENST00000245907.10:c.3970-15_3970-13delinsCTT	ENSP00000245907.4:n.3970-15_3970-13delinsCTT
ENST00000596238.1:n.413-15_413-13delinsCTT
ENST00000596548.1:c.52-15_52-13delinsCTT	ENSP00000469744.1:n.52-15_52-13delinsCTT
ENST00000601008.1:c.241+1897_241+1899delinsCTT	ENSP00000471384.1:n.241+1897_241+1899delinsCTT
NM_000064.3:c.3970-15_3970-13delinsCTT	NP_000055.2:n.3970-15_3970-13delinsCTT
NM_000064.4:c.3970-15_3970-13delinsCTT MANE Select	NP_000055.2:n.3970-15_3970-13delinsCTT