Canonical Allele Identifier: CA1147954630
Gene: FH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241504029G= , CM000663.2:g.241504029G= GRCh38
NC_000001.10:g.241667329G= , CM000663.1:g.241667329G= GRCh37
NC_000001.9:g.239733952G= NCBI36
NG_012338.1:g.20726C= , LRG_504:g.20726C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000493477.2:n.1611+13C=
ENST00000682162.1:c.1137+13C= ENSP00000508203.1:n.1137+13C=
ENST00000682567.1:n.1198C=
ENST00000683521.1:c.1108+13C= ENSP00000506864.1:n.1108+13C=
ENST00000684161.1:n.2323+13C=
ENST00000684483.1:c.*504+13C= ENSP00000507894.1:n.*504+13C=
ENST00000366560.4:c.1108+13C= MANE Select ENSP00000355518.4:n.1108+13C=
ENST00000366560.3:c.1108+13C= ENSP00000355518.3:n.1108+13C=
NM_000143.3:c.1108+13C= , LRG_504t1:c.1108+13C= NP_000134.2:n.1108+13C=
XM_011544132.1:c.880+13C= XP_011542434.1:n.880+13C=
XM_011544132.2:c.880+13C= XP_011542434.1:n.880+13C=
NM_000143.4:c.1108+13C= MANE Select NP_000134.2:n.1108+13C=