Canonical Allele Identifier: CA1229578321

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502917A= , CM000663.2:g.241502917A=	GRCh38
NC_000001.10:g.241666217A= , CM000663.1:g.241666217A=	GRCh37
NC_000001.9:g.239732840A=	NCBI36
NG_012338.1:g.21838T= , LRG_504:g.21838T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1612-347T=
ENST00000682162.1:c.1138-347T=	ENSP00000508203.1:n.1138-347T=
ENST00000682567.1:n.2310T=
ENST00000683521.1:c.1109-347T=	ENSP00000506864.1:n.1109-347T=
ENST00000684161.1:n.2324-347T=
ENST00000684483.1:c.*505-347T=	ENSP00000507894.1:n.*505-347T=
ENST00000366560.4:c.1109-347T= MANE Select	ENSP00000355518.4:n.1109-347T=
ENST00000366560.3:c.1109-347T=	ENSP00000355518.3:n.1109-347T=
NM_000143.3:c.1109-347T= , LRG_504t1:c.1109-347T=	NP_000134.2:n.1109-347T=
XM_011544132.1:c.881-347T=	XP_011542434.1:n.881-347T=
XM_011544132.2:c.881-347T=	XP_011542434.1:n.881-347T=
NM_000143.4:c.1109-347T= MANE Select	NP_000134.2:n.1109-347T=