Canonical Allele Identifier: CA1876865798
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120962668T= , CM000671.2:g.120962668T= GRCh38
NC_000009.11:g.123724946T= , CM000671.1:g.123724946T= GRCh37
NC_000009.10:g.122764767T= NCBI36
NG_007364.1:g.92609A= , LRG_28:g.92609A=

Transcript Alleles

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