Canonical Allele Identifier: CA1229580765

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508911G= , CM000663.2:g.241508911G=	GRCh38
NC_000001.10:g.241672211G= , CM000663.1:g.241672211G=	GRCh37
NC_000001.9:g.239738834G=	NCBI36
NG_012338.1:g.15844C= , LRG_504:g.15844C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1059-126C=
ENST00000682162.1:c.585-126C=	ENSP00000508203.1:n.585-126C=
ENST00000682567.1:n.633-126C=
ENST00000683521.1:c.556-126C=	ENSP00000506864.1:n.556-126C=
ENST00000684161.1:n.1645C=
ENST00000684483.1:c.556-151C=	ENSP00000507894.1:n.556-151C=
ENST00000366560.4:c.556-126C= MANE Select	ENSP00000355518.4:n.556-126C=
ENST00000366560.3:c.556-126C=	ENSP00000355518.3:n.556-126C=
NM_000143.3:c.556-126C= , LRG_504t1:c.556-126C=	NP_000134.2:n.556-126C=
XM_011544132.1:c.328-126C=	XP_011542434.1:n.328-126C=
XM_011544132.2:c.328-126C=	XP_011542434.1:n.328-126C=
NM_000143.4:c.556-126C= MANE Select	NP_000134.2:n.556-126C=