Canonical Allele Identifier: CA1229580618
Gene: FH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241508610A= , CM000663.2:g.241508610A= GRCh38
NC_000001.10:g.241671910A= , CM000663.1:g.241671910A= GRCh37
NC_000001.9:g.239738533A= NCBI36
NG_012338.1:g.16145T= , LRG_504:g.16145T=

Transcript Alleles

HGVS Amino-acid change
ENST00000493477.2:n.1234T=
ENST00000682162.1:c.760T= ENSP00000508203.1:n.760T=
ENST00000682567.1:n.808T=
ENST00000683521.1:c.731T= ENSP00000506864.1:p.Leu244=
ENST00000684161.1:n.1946T=
ENST00000684483.1:c.*127T= ENSP00000507894.1:n.*127T=
ENST00000366560.4:c.731T= MANE Select ENSP00000355518.4:p.Leu244=
ENST00000366560.3:c.731T= ENSP00000355518.3:p.Leu244=
NM_000143.3:c.731T= , LRG_504t1:c.731T= NP_000134.2:p.Leu244=
XM_011544132.1:c.503T= XP_011542434.1:p.Leu168=
XM_011544132.2:c.503T= XP_011542434.1:p.Leu168=
NM_000143.4:c.731T= MANE Select NP_000134.2:p.Leu244=