Canonical Allele Identifier: CA2320553324
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6685916_6685918delinsAAC , CM000681.2:g.6685916_6685918delinsAAC GRCh38
NC_000019.9:g.6685927_6685929delinsAAC , CM000681.1:g.6685927_6685929delinsAAC GRCh37
NC_000019.8:g.6636927_6636929delinsAAC NCBI36
NG_009557.1:g.39734_39736delinsGTT , LRG_27:g.39734_39736delinsGTT

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.2158+206_2158+208delinsGTT
ENST00000695653.1:c.1719+206_1719+208delinsGTT ENSP00000512084.1:n.1719+206_1719+208deli...
ENST00000695654.1:c.2835+206_2835+208delinsGTT ENSP00000512085.1:n.2835+206_2835+208deli...
ENST00000245907.11:c.3810+206_3810+208delinsGTT MANE Select ENSP00000245907.4:n.3810+206_3810+208deli...
ENST00000245907.10:c.3810+206_3810+208delinsGTT ENSP00000245907.4:n.3810+206_3810+208deli...
ENST00000596238.1:n.253+206_253+208delinsGTT
ENST00000601008.1:c.241+828_241+830delinsGTT ENSP00000471384.1:n.241+828_241+830delins...
NM_000064.3:c.3810+206_3810+208delinsGTT NP_000055.2:n.3810+206_3810+208delinsGTT
NM_000064.4:c.3810+206_3810+208delinsGTT MANE Select NP_000055.2:n.3810+206_3810+208delinsGTT