Canonical Allele Identifier: CA1876874454
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120980588_120980589delinsTC , CM000671.2:g.120980588_120980589delinsTC GRCh38
NC_000009.11:g.123742866_123742867delinsTC , CM000671.1:g.123742866_123742867delinsTC GRCh37
NC_000009.10:g.122782687_122782688delinsTC NCBI36
NG_007364.1:g.74688_74689delinsGA , LRG_28:g.74688_74689delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000480188.2:n.398-335_398-334delinsGA
ENST00000696279.1:c.3807-335_3807-334delinsGA
ENST00000696280.1:n.3576-335_3576-334delinsGA
ENST00000696281.1:c.3505-335_3505-334delinsGA ENSP00000512521.1:n.3505-335_3505-334deli...
ENST00000697921.1:n.2365-335_2365-334delinsGA
ENST00000697922.1:c.*3477-335_*3477-334delinsGA ENSP00000513478.1:n.*3477-335_*3477-334de...
ENST00000697923.1:n.3932-335_3932-334delinsGA
ENST00000223642.3:c.3487-335_3487-334delinsGA MANE Select ENSP00000223642.1:n.3487-335_3487-334deli...
ENST00000223642.2:c.3487-335_3487-334delinsGA ENSP00000223642.1:n.3487-335_3487-334deli...
ENST00000489802.1:n.50-335_50-334delinsGA
NM_001735.2:c.3487-335_3487-334delinsGA , LRG_28t1:c.3487-335_3487-334delinsGA NP_001726.2:n.3487-335_3487-334delinsGA
XM_011518980.1:c.3502-335_3502-334delinsGA XP_011517282.1:n.3502-335_3502-334delinsG...
NM_001317163.1:c.3505-335_3505-334delinsGA NP_001304092.1:n.3505-335_3505-334delinsG...
NM_001317163.2:c.3505-335_3505-334delinsGA NP_001304092.1:n.3505-335_3505-334delinsG...
NM_001735.3:c.3487-335_3487-334delinsGA MANE Select NP_001726.2:n.3487-335_3487-334delinsGA