Canonical Allele Identifier: CA2320559281
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697900_6697901delinsCA , CM000681.2:g.6697900_6697901delinsCA GRCh38
NC_000019.9:g.6697911_6697912delinsCA , CM000681.1:g.6697911_6697912delinsCA GRCh37
NC_000019.8:g.6648911_6648912delinsCA NCBI36
NG_009557.1:g.27751_27752delinsTG , LRG_27:g.27751_27752delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.789-107_789-106delinsTG
ENST00000695652.1:c.2318-107_2318-106delinsTG ENSP00000512083.1:n.2318-107_2318-106delinsTG
ENST00000695653.1:c.350-107_350-106delinsTG ENSP00000512084.1:n.350-107_350-106delinsTG
ENST00000695654.1:c.1565-107_1565-106delinsTG ENSP00000512085.1:n.1565-107_1565-106delinsTG
ENST00000695655.1:c.1382-107_1382-106delinsTG ENSP00000512086.1:n.1382-107_1382-106delinsTG
ENST00000695692.1:n.1805-107_1805-106delinsTG
ENST00000245907.11:c.2441-107_2441-106delinsTG MANE Select ENSP00000245907.4:n.2441-107_2441-106delinsTG
ENST00000245907.10:c.2441-107_2441-106delinsTG ENSP00000245907.4:n.2441-107_2441-106delinsTG
ENST00000602053.1:n.489-107_489-106delinsTG
NM_000064.3:c.2441-107_2441-106delinsTG NP_000055.2:n.2441-107_2441-106delinsTG
NM_000064.4:c.2441-107_2441-106delinsTG MANE Select NP_000055.2:n.2441-107_2441-106delinsTG