Canonical Allele Identifier: CA1876865623
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120962223T= , CM000671.2:g.120962223T= GRCh38
NC_000009.11:g.123724501T= , CM000671.1:g.123724501T= GRCh37
NC_000009.10:g.122764322T= NCBI36
NG_007364.1:g.93054A= , LRG_28:g.93054A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000480188.2:n.1538+448A=
ENST00000696279.1:c.4824+448A=
ENST00000696280.1:n.4593+448A=
ENST00000696281.1:c.4522+448A= ENSP00000512521.1:n.4522+448A=
ENST00000697921.1:n.3382+448A=
ENST00000697922.1:c.*4494+448A= ENSP00000513478.1:n.*4494+448A=
ENST00000697923.1:n.4949+448A=
ENST00000223642.3:c.4504+448A= MANE Select ENSP00000223642.1:n.4504+448A=
ENST00000223642.2:c.4504+448A= ENSP00000223642.1:n.4504+448A=
ENST00000480188.1:n.37+448A=
NM_001735.2:c.4504+448A= , LRG_28t1:c.4504+448A= NP_001726.2:n.4504+448A=
XM_011518980.1:c.4519+448A= XP_011517282.1:n.4519+448A=
NM_001317163.1:c.4522+448A= NP_001304092.1:n.4522+448A=
NM_001317163.2:c.4522+448A= NP_001304092.1:n.4522+448A=
NM_001735.3:c.4504+448A= MANE Select NP_001726.2:n.4504+448A=