Canonical Allele Identifier: CA1876884256
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.121006787A= , CM000671.2:g.121006787A= GRCh38
NC_000009.11:g.123769065A= , CM000671.1:g.123769065A= GRCh37
NC_000009.10:g.122808886A= NCBI36
NG_007364.1:g.48490T= , LRG_28:g.48490T=

Transcript Alleles

HGVS Amino-acid change
ENST00000466280.2:c.1417+117T= ENSP00000513491.1:n.1417+117T=
ENST00000696279.1:c.2742+117T=
ENST00000696280.1:n.2511+117T=
ENST00000696281.1:c.2440+117T= ENSP00000512521.1:n.2440+117T=
ENST00000697921.1:n.1300+117T=
ENST00000697922.1:c.*2412+117T= ENSP00000513478.1:n.*2412+117T=
ENST00000697923.1:n.3027+117T=
ENST00000223642.3:c.2422+117T= MANE Select ENSP00000223642.1:n.2422+117T=
ENST00000223642.2:c.2422+117T= ENSP00000223642.1:n.2422+117T=
ENST00000466280.1:n.25+117T=
NM_001735.2:c.2422+117T= , LRG_28t1:c.2422+117T= NP_001726.2:n.2422+117T=
XM_011518980.1:c.2437+117T= XP_011517282.1:n.2437+117T=
XM_011518981.1:c.2440+117T= XP_011517283.1:n.2440+117T=
NM_001317163.1:c.2440+117T= NP_001304092.1:n.2440+117T=
NM_001317164.1:c.2422+117T= NP_001304093.1:n.2422+117T=
NM_001317163.2:c.2440+117T= NP_001304092.1:n.2440+117T=
NM_001317164.2:c.2422+117T= NP_001304093.1:n.2422+117T=
NM_001735.3:c.2422+117T= MANE Select NP_001726.2:n.2422+117T=