Canonical Allele Identifier: CA1876865828
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120962758G= , CM000671.2:g.120962758G= GRCh38
NC_000009.11:g.123725036G= , CM000671.1:g.123725036G= GRCh37
NC_000009.10:g.122764857G= NCBI36
NG_007364.1:g.92519C= , LRG_28:g.92519C=

Transcript Alleles

HGVS Amino-acid change
ENST00000480188.2:n.1451C=
ENST00000696279.1:c.4737C=
ENST00000696280.1:n.4506C=
ENST00000696281.1:c.4435C= ENSP00000512521.1:p.Leu1479=
ENST00000697921.1:n.3295C=
ENST00000697922.1:c.*4407C= ENSP00000513478.1:n.*4407C=
ENST00000697923.1:n.4862C=
ENST00000223642.3:c.4417C= MANE Select ENSP00000223642.1:p.Leu1473=
ENST00000223642.2:c.4417C= ENSP00000223642.1:p.Leu1473=
NM_001735.2:c.4417C= , LRG_28t1:c.4417C= NP_001726.2:p.Leu1473=
XM_011518980.1:c.4432C= XP_011517282.1:p.Leu1478=
NM_001317163.1:c.4435C= NP_001304092.1:p.Leu1479=
NM_001317163.2:c.4435C= NP_001304092.1:p.Leu1479=
NM_001735.3:c.4417C= MANE Select NP_001726.2:p.Leu1473=