Canonical Allele Identifier: CA1876884281
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.121006861T= , CM000671.2:g.121006861T= GRCh38
NC_000009.11:g.123769139T= , CM000671.1:g.123769139T= GRCh37
NC_000009.10:g.122808960T= NCBI36
NG_007364.1:g.48416A= , LRG_28:g.48416A=

Transcript Alleles

HGVS Amino-acid change
ENST00000466280.2:c.1417+43A= ENSP00000513491.1:n.1417+43A=
ENST00000696279.1:c.2742+43A=
ENST00000696280.1:n.2511+43A=
ENST00000696281.1:c.2440+43A= ENSP00000512521.1:n.2440+43A=
ENST00000697921.1:n.1300+43A=
ENST00000697922.1:c.*2412+43A= ENSP00000513478.1:n.*2412+43A=
ENST00000697923.1:n.3027+43A=
ENST00000223642.3:c.2422+43A= MANE Select ENSP00000223642.1:n.2422+43A=
ENST00000223642.2:c.2422+43A= ENSP00000223642.1:n.2422+43A=
ENST00000466280.1:n.25+43A=
NM_001735.2:c.2422+43A= , LRG_28t1:c.2422+43A= NP_001726.2:n.2422+43A=
XM_011518980.1:c.2437+43A= XP_011517282.1:n.2437+43A=
XM_011518981.1:c.2440+43A= XP_011517283.1:n.2440+43A=
NM_001317163.1:c.2440+43A= NP_001304092.1:n.2440+43A=
NM_001317164.1:c.2422+43A= NP_001304093.1:n.2422+43A=
NM_001317163.2:c.2440+43A= NP_001304092.1:n.2440+43A=
NM_001317164.2:c.2422+43A= NP_001304093.1:n.2422+43A=
NM_001735.3:c.2422+43A= MANE Select NP_001726.2:n.2422+43A=