Canonical Allele Identifier: CA1229578175
Gene: FH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241502569G= , CM000663.2:g.241502569G= GRCh38
NC_000001.10:g.241665869G= , CM000663.1:g.241665869G= GRCh37
NC_000001.9:g.239732492G= NCBI36
NG_012338.1:g.22186C= , LRG_504:g.22186C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000493477.2:n.1613C=
ENST00000682162.1:c.1139C= ENSP00000508203.1:n.1139C=
ENST00000682567.1:n.2658C=
ENST00000683521.1:c.1110C= ENSP00000506864.1:p.Gly370=
ENST00000684161.1:n.2325C=
ENST00000684483.1:c.*506C= ENSP00000507894.1:n.*506C=
ENST00000366560.4:c.1110C= MANE Select ENSP00000355518.4:p.Gly370=
ENST00000366560.3:c.1110C= ENSP00000355518.3:p.Gly370=
NM_000143.3:c.1110C= , LRG_504t1:c.1110C= NP_000134.2:p.Gly370=
XM_011544132.1:c.882C= XP_011542434.1:p.Gly294=
XM_011544132.2:c.882C= XP_011542434.1:p.Gly294=
NM_000143.4:c.1110C= MANE Select NP_000134.2:p.Gly370=