Canonical Allele Identifier: CA1876865769
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120962590C= , CM000671.2:g.120962590C= GRCh38
NC_000009.11:g.123724868C= , CM000671.1:g.123724868C= GRCh37
NC_000009.10:g.122764689C= NCBI36
NG_007364.1:g.92687G= , LRG_28:g.92687G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000480188.2:n.1538+81G=
ENST00000696279.1:c.4824+81G=
ENST00000696280.1:n.4593+81G=
ENST00000696281.1:c.4522+81G= ENSP00000512521.1:n.4522+81G=
ENST00000697921.1:n.3382+81G=
ENST00000697922.1:c.*4494+81G= ENSP00000513478.1:n.*4494+81G=
ENST00000697923.1:n.4949+81G=
ENST00000223642.3:c.4504+81G= MANE Select ENSP00000223642.1:n.4504+81G=
ENST00000223642.2:c.4504+81G= ENSP00000223642.1:n.4504+81G=
ENST00000480188.1:n.37+81G=
NM_001735.2:c.4504+81G= , LRG_28t1:c.4504+81G= NP_001726.2:n.4504+81G=
XM_011518980.1:c.4519+81G= XP_011517282.1:n.4519+81G=
NM_001317163.1:c.4522+81G= NP_001304092.1:n.4522+81G=
NM_001317163.2:c.4522+81G= NP_001304092.1:n.4522+81G=
NM_001735.3:c.4504+81G= MANE Select NP_001726.2:n.4504+81G=