Canonical Allele Identifier: CA1876862588
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120954546A= , CM000671.2:g.120954546A= GRCh38
NC_000009.11:g.123716824A= , CM000671.1:g.123716824A= GRCh37
NC_000009.10:g.122756645A= NCBI36
NG_007364.1:g.100731T= , LRG_28:g.100731T=

Transcript Alleles

HGVS Amino-acid change
ENST00000480188.2:n.4535T=
ENST00000696279.1:c.5083-678T=
ENST00000696280.1:n.4852-678T=
ENST00000696281.1:c.4781-678T= ENSP00000512521.1:n.4781-678T=
ENST00000697921.1:n.3641-678T=
ENST00000697922.1:c.*4753-678T= ENSP00000513478.1:n.*4753-678T=
ENST00000697923.1:n.7946T=
ENST00000223642.3:c.4763-678T= MANE Select ENSP00000223642.1:n.4763-678T=
ENST00000223642.2:c.4763-678T= ENSP00000223642.1:n.4763-678T=
NM_001735.2:c.4763-678T= , LRG_28t1:c.4763-678T= NP_001726.2:n.4763-678T=
XM_011518980.1:c.4778-678T= XP_011517282.1:n.4778-678T=
NM_001317163.1:c.4781-678T= NP_001304092.1:n.4781-678T=
NM_001317163.2:c.4781-678T= NP_001304092.1:n.4781-678T=
NM_001735.3:c.4763-678T= MANE Select NP_001726.2:n.4763-678T=