Canonical Allele Identifier: CA2320567875
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713341_6713342delinsGA , CM000681.2:g.6713341_6713342delinsGA GRCh38
NC_000019.9:g.6713352_6713353delinsGA , CM000681.1:g.6713352_6713353delinsGA GRCh37
NC_000019.8:g.6664352_6664353delinsGA NCBI36
NG_009557.1:g.12310_12311delinsTC , LRG_27:g.12310_12311delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.754-27_754-26delinsTC ENSP00000512083.1:n.754-27_754-26delinsTC
ENST00000695692.1:n.201-27_201-26delinsTC
ENST00000245907.11:c.877-27_877-26delinsTC MANE Select ENSP00000245907.4:n.877-27_877-26delinsTC
ENST00000245907.10:c.877-27_877-26delinsTC ENSP00000245907.4:n.877-27_877-26delinsTC
ENST00000595577.1:n.381-27_381-26delinsTC
ENST00000597442.5:n.127-27_127-26delinsTC
NM_000064.3:c.877-27_877-26delinsTC NP_000055.2:n.877-27_877-26delinsTC
NM_000064.4:c.877-27_877-26delinsTC MANE Select NP_000055.2:n.877-27_877-26delinsTC