Canonical Allele Identifier: CA1876874440
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120980573A= , CM000671.2:g.120980573A= GRCh38
NC_000009.11:g.123742851A= , CM000671.1:g.123742851A= GRCh37
NC_000009.10:g.122782672A= NCBI36
NG_007364.1:g.74704T= , LRG_28:g.74704T=

Transcript Alleles

HGVS Amino-acid change
ENST00000480188.2:n.398-319T=
ENST00000696279.1:c.3807-319T=
ENST00000696280.1:n.3576-319T=
ENST00000696281.1:c.3505-319T= ENSP00000512521.1:n.3505-319T=
ENST00000697921.1:n.2365-319T=
ENST00000697922.1:c.*3477-319T= ENSP00000513478.1:n.*3477-319T=
ENST00000697923.1:n.3932-319T=
ENST00000223642.3:c.3487-319T= MANE Select ENSP00000223642.1:n.3487-319T=
ENST00000223642.2:c.3487-319T= ENSP00000223642.1:n.3487-319T=
ENST00000489802.1:n.50-319T=
NM_001735.2:c.3487-319T= , LRG_28t1:c.3487-319T= NP_001726.2:n.3487-319T=
XM_011518980.1:c.3502-319T= XP_011517282.1:n.3502-319T=
NM_001317163.1:c.3505-319T= NP_001304092.1:n.3505-319T=
NM_001317163.2:c.3505-319T= NP_001304092.1:n.3505-319T=
NM_001735.3:c.3487-319T= MANE Select NP_001726.2:n.3487-319T=