Canonical Allele Identifier: CA1229578122
Gene: FH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241502467C= , CM000663.2:g.241502467C= GRCh38
NC_000001.10:g.241665767C= , CM000663.1:g.241665767C= GRCh37
NC_000001.9:g.239732390C= NCBI36
NG_012338.1:g.22288G= , LRG_504:g.22288G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000493477.2:n.1715G=
ENST00000682162.1:c.1241G= ENSP00000508203.1:n.1241G=
ENST00000682567.1:n.2760G=
ENST00000683521.1:c.1212G= ENSP00000506864.1:p.Glu404=
ENST00000684161.1:n.2427G=
ENST00000684483.1:c.*608G= ENSP00000507894.1:n.*608G=
ENST00000366560.4:c.1212G= MANE Select ENSP00000355518.4:p.Glu404=
ENST00000366560.3:c.1212G= ENSP00000355518.3:p.Glu404=
NM_000143.3:c.1212G= , LRG_504t1:c.1212G= NP_000134.2:p.Glu404=
XM_011544132.1:c.984G= XP_011542434.1:p.Glu328=
XM_011544132.2:c.984G= XP_011542434.1:p.Glu328=
NM_000143.4:c.1212G= MANE Select NP_000134.2:p.Glu404=