Canonical Allele Identifier: CA2320561788

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6701439_6701441delinsTAA , CM000681.2:g.6701439_6701441delinsTAA	GRCh38
NC_000019.9:g.6701450_6701452delinsTAA , CM000681.1:g.6701450_6701452delinsTAA	GRCh37
NC_000019.8:g.6652450_6652452delinsTAA	NCBI36
NG_009557.1:g.24211_24213delinsTTA , LRG_27:g.24211_24213delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.788+686_788+688delinsTTA
ENST00000695652.1:c.2317+686_2317+688delinsTTA	ENSP00000512083.1:n.2317+686_2317+688delinsTTA
ENST00000695653.1:c.349+686_349+688delinsTTA	ENSP00000512084.1:n.349+686_349+688delinsTTA
ENST00000695654.1:c.1564+686_1564+688delinsTTA	ENSP00000512085.1:n.1564+686_1564+688delinsTTA
ENST00000695655.1:c.1381+686_1381+688delinsTTA	ENSP00000512086.1:n.1381+686_1381+688delinsTTA
ENST00000695692.1:n.1804+686_1804+688delinsTTA
ENST00000245907.11:c.2440+686_2440+688delinsTTA MANE Select	ENSP00000245907.4:n.2440+686_2440+688delinsTTA
ENST00000245907.10:c.2440+686_2440+688delinsTTA	ENSP00000245907.4:n.2440+686_2440+688delinsTTA
ENST00000602053.1:n.488+686_488+688delinsTTA
NM_000064.3:c.2440+686_2440+688delinsTTA	NP_000055.2:n.2440+686_2440+688delinsTTA
NM_000064.4:c.2440+686_2440+688delinsTTA MANE Select	NP_000055.2:n.2440+686_2440+688delinsTTA