Canonical Allele Identifier: CA1876870711
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120974766G= , CM000671.2:g.120974766G= GRCh38
NC_000009.11:g.123737044G= , CM000671.1:g.123737044G= GRCh37
NC_000009.10:g.122776865G= NCBI36
NG_007364.1:g.80511C= , LRG_28:g.80511C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000480188.2:n.928+13C=
ENST00000696279.1:c.4337+13C=
ENST00000696280.1:n.4106+13C=
ENST00000696281.1:c.4035+13C= ENSP00000512521.1:n.4035+13C=
ENST00000697921.1:n.2895+13C=
ENST00000697922.1:c.*4007+13C= ENSP00000513478.1:n.*4007+13C=
ENST00000697923.1:n.4462+13C=
ENST00000223642.3:c.4017+13C= MANE Select ENSP00000223642.1:n.4017+13C=
ENST00000223642.2:c.4017+13C= ENSP00000223642.1:n.4017+13C=
NM_001735.2:c.4017+13C= , LRG_28t1:c.4017+13C= NP_001726.2:n.4017+13C=
XM_011518980.1:c.4032+13C= XP_011517282.1:n.4032+13C=
NM_001317163.1:c.4035+13C= NP_001304092.1:n.4035+13C=
NM_001317163.2:c.4035+13C= NP_001304092.1:n.4035+13C=
NM_001735.3:c.4017+13C= MANE Select NP_001726.2:n.4017+13C=