Canonical Allele Identifier: CA1229577266
Gene: FH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241500465C= , CM000663.2:g.241500465C= GRCh38
NC_000001.10:g.241663765C= , CM000663.1:g.241663765C= GRCh37
NC_000001.9:g.239730388C= NCBI36
NG_012338.1:g.24290G= , LRG_504:g.24290G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000493477.2:n.1865G=
ENST00000682162.1:c.1391G= ENSP00000508203.1:n.1391G=
ENST00000682567.1:n.4762G=
ENST00000683521.1:c.1362G= ENSP00000506864.1:p.Met454=
ENST00000684161.1:n.2577G=
ENST00000684483.1:c.*758G= ENSP00000507894.1:n.*758G=
ENST00000366560.4:c.1362G= MANE Select ENSP00000355518.4:p.Met454=
ENST00000366560.3:c.1362G= ENSP00000355518.3:p.Met454=
NM_000143.3:c.1362G= , LRG_504t1:c.1362G= NP_000134.2:p.Met454=
XM_011544132.1:c.1134G= XP_011542434.1:p.Met378=
XM_011544132.2:c.1134G= XP_011542434.1:p.Met378=
NM_000143.4:c.1362G= MANE Select NP_000134.2:p.Met454=