Canonical Allele Identifier: CA1229580616
Gene: FH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241508608C= , CM000663.2:g.241508608C= GRCh38
NC_000001.10:g.241671908C= , CM000663.1:g.241671908C= GRCh37
NC_000001.9:g.239738531C= NCBI36
NG_012338.1:g.16147G= , LRG_504:g.16147G=

Transcript Alleles

HGVS Amino-acid change
ENST00000493477.2:n.1236G=
ENST00000682162.1:c.762G= ENSP00000508203.1:n.762G=
ENST00000682567.1:n.810G=
ENST00000683521.1:c.733G= ENSP00000506864.1:p.Gly245=
ENST00000684161.1:n.1948G=
ENST00000684483.1:c.*129G= ENSP00000507894.1:n.*129G=
ENST00000366560.4:c.733G= MANE Select ENSP00000355518.4:p.Gly245=
ENST00000366560.3:c.733G= ENSP00000355518.3:p.Gly245=
NM_000143.3:c.733G= , LRG_504t1:c.733G= NP_000134.2:p.Gly245=
XM_011544132.1:c.505G= XP_011542434.1:p.Gly169=
XM_011544132.2:c.505G= XP_011542434.1:p.Gly169=
NM_000143.4:c.733G= MANE Select NP_000134.2:p.Gly245=