Canonical Allele Identifier: CA1229578778

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504058T= , CM000663.2:g.241504058T=	GRCh38
NC_000001.10:g.241667358T= , CM000663.1:g.241667358T=	GRCh37
NC_000001.9:g.239733981T=	NCBI36
NG_012338.1:g.20697A= , LRG_504:g.20697A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1595A=
ENST00000682162.1:c.1121A=	ENSP00000508203.1:n.1121A=
ENST00000682567.1:n.1169A=
ENST00000683521.1:c.1092A=	ENSP00000506864.1:p.Gly364=
ENST00000684161.1:n.2307A=
ENST00000684483.1:c.*488A=	ENSP00000507894.1:n.*488A=
ENST00000366560.4:c.1092A= MANE Select	ENSP00000355518.4:p.Gly364=
ENST00000366560.3:c.1092A=	ENSP00000355518.3:p.Gly364=
NM_000143.3:c.1092A= , LRG_504t1:c.1092A=	NP_000134.2:p.Gly364=
XM_011544132.1:c.864A=	XP_011542434.1:p.Gly288=
XM_011544132.2:c.864A=	XP_011542434.1:p.Gly288=
NM_000143.4:c.1092A= MANE Select	NP_000134.2:p.Gly364=