Canonical Allele Identifier: CA1876865829
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120962760A= , CM000671.2:g.120962760A= GRCh38
NC_000009.11:g.123725038A= , CM000671.1:g.123725038A= GRCh37
NC_000009.10:g.122764859A= NCBI36
NG_007364.1:g.92517T= , LRG_28:g.92517T=

Transcript Alleles

HGVS Amino-acid change
ENST00000480188.2:n.1449T=
ENST00000696279.1:c.4735T=
ENST00000696280.1:n.4504T=
ENST00000696281.1:c.4433T= ENSP00000512521.1:p.Phe1478=
ENST00000697921.1:n.3293T=
ENST00000697922.1:c.*4405T= ENSP00000513478.1:n.*4405T=
ENST00000697923.1:n.4860T=
ENST00000223642.3:c.4415T= MANE Select ENSP00000223642.1:p.Phe1472=
ENST00000223642.2:c.4415T= ENSP00000223642.1:p.Phe1472=
NM_001735.2:c.4415T= , LRG_28t1:c.4415T= NP_001726.2:p.Phe1472=
XM_011518980.1:c.4430T= XP_011517282.1:p.Phe1477=
NM_001317163.1:c.4433T= NP_001304092.1:p.Phe1478=
NM_001317163.2:c.4433T= NP_001304092.1:p.Phe1478=
NM_001735.3:c.4415T= MANE Select NP_001726.2:p.Phe1472=