Canonical Allele Identifier: CA2320553423
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6686099_6686100delinsGC , CM000681.2:g.6686099_6686100delinsGC GRCh38
NC_000019.9:g.6686110_6686111delinsGC , CM000681.1:g.6686110_6686111delinsGC GRCh37
NC_000019.8:g.6637110_6637111delinsGC NCBI36
NG_009557.1:g.39552_39553delinsGC , LRG_27:g.39552_39553delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.2158+24_2158+25delinsGC
ENST00000695653.1:c.1719+24_1719+25delinsGC ENSP00000512084.1:n.1719+24_1719+25delinsGC
ENST00000695654.1:c.2835+24_2835+25delinsGC ENSP00000512085.1:n.2835+24_2835+25delinsGC
ENST00000245907.11:c.3810+24_3810+25delinsGC MANE Select ENSP00000245907.4:n.3810+24_3810+25delinsGC
ENST00000245907.10:c.3810+24_3810+25delinsGC ENSP00000245907.4:n.3810+24_3810+25delinsGC
ENST00000596238.1:n.253+24_253+25delinsGC
ENST00000601008.1:c.241+646_241+647delinsGC ENSP00000471384.1:n.241+646_241+647delinsGC
NM_000064.3:c.3810+24_3810+25delinsGC NP_000055.2:n.3810+24_3810+25delinsGC
NM_000064.4:c.3810+24_3810+25delinsGC MANE Select NP_000055.2:n.3810+24_3810+25delinsGC