Canonical Allele Identifier: CA2320559155
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697629_6697630delinsGC , CM000681.2:g.6697629_6697630delinsGC GRCh38
NC_000019.9:g.6697640_6697641delinsGC , CM000681.1:g.6697640_6697641delinsGC GRCh37
NC_000019.8:g.6648640_6648641delinsGC NCBI36
NG_009557.1:g.28022_28023delinsGC , LRG_27:g.28022_28023delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.931+22_931+23delinsGC
ENST00000695652.1:c.2460+22_2460+23delinsGC ENSP00000512083.1:n.2460+22_2460+23delinsGC
ENST00000695653.1:c.492+22_492+23delinsGC ENSP00000512084.1:n.492+22_492+23delinsGC
ENST00000695654.1:c.1707+22_1707+23delinsGC ENSP00000512085.1:n.1707+22_1707+23delinsGC
ENST00000695655.1:c.1524+22_1524+23delinsGC ENSP00000512086.1:n.1524+22_1524+23delinsGC
ENST00000695692.1:n.1947+22_1947+23delinsGC
ENST00000245907.11:c.2583+22_2583+23delinsGC MANE Select ENSP00000245907.4:n.2583+22_2583+23delinsGC
ENST00000245907.10:c.2583+22_2583+23delinsGC ENSP00000245907.4:n.2583+22_2583+23delinsGC
ENST00000594005.1:n.86_87delinsGC
NM_000064.3:c.2583+22_2583+23delinsGC NP_000055.2:n.2583+22_2583+23delinsGC
NM_000064.4:c.2583+22_2583+23delinsGC MANE Select NP_000055.2:n.2583+22_2583+23delinsGC