Canonical Allele Identifier: CA1876874470
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120980595T= , CM000671.2:g.120980595T= GRCh38
NC_000009.11:g.123742873T= , CM000671.1:g.123742873T= GRCh37
NC_000009.10:g.122782694T= NCBI36
NG_007364.1:g.74682A= , LRG_28:g.74682A=

Transcript Alleles

HGVS Amino-acid change
ENST00000480188.2:n.398-341A=
ENST00000696279.1:c.3807-341A=
ENST00000696280.1:n.3576-341A=
ENST00000696281.1:c.3505-341A= ENSP00000512521.1:n.3505-341A=
ENST00000697921.1:n.2365-341A=
ENST00000697922.1:c.*3477-341A= ENSP00000513478.1:n.*3477-341A=
ENST00000697923.1:n.3932-341A=
ENST00000223642.3:c.3487-341A= MANE Select ENSP00000223642.1:n.3487-341A=
ENST00000223642.2:c.3487-341A= ENSP00000223642.1:n.3487-341A=
ENST00000489802.1:n.50-341A=
NM_001735.2:c.3487-341A= , LRG_28t1:c.3487-341A= NP_001726.2:n.3487-341A=
XM_011518980.1:c.3502-341A= XP_011517282.1:n.3502-341A=
NM_001317163.1:c.3505-341A= NP_001304092.1:n.3505-341A=
NM_001317163.2:c.3505-341A= NP_001304092.1:n.3505-341A=
NM_001735.3:c.3487-341A= MANE Select NP_001726.2:n.3487-341A=