Canonical Allele Identifier: CA345437307
Gene: FH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241502468T>G , CM000663.2:g.241502468T>G GRCh38
NC_000001.10:g.241665768T>G , CM000663.1:g.241665768T>G GRCh37
NC_000001.9:g.239732391T>G NCBI36
NG_012338.1:g.22287A>C , LRG_504:g.22287A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000493477.2:n.1714A>C
ENST00000682162.1:c.1240A>C ENSP00000508203.1:n.1240A>C
ENST00000682567.1:n.2759A>C
ENST00000683521.1:c.1211A>C ENSP00000506864.1:p.Glu404Ala
ENST00000684161.1:n.2426A>C
ENST00000684483.1:c.*607A>C ENSP00000507894.1:n.*607A>C
ENST00000366560.4:c.1211A>C MANE Select ENSP00000355518.4:p.Glu404Ala
ENST00000366560.3:c.1211A>C ENSP00000355518.3:p.Glu404Ala
NM_000143.3:c.1211A>C , LRG_504t1:c.1211A>C NP_000134.2:p.Glu404Ala
XM_011544132.1:c.983A>C XP_011542434.1:p.Glu328Ala
XM_011544132.2:c.983A>C XP_011542434.1:p.Glu328Ala
NM_000143.4:c.1211A>C MANE Select NP_000134.2:p.Glu404Ala