Canonical Allele Identifier: CA1145074947

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508924G= , CM000663.2:g.241508924G=	GRCh38
NC_000001.10:g.241672224G= , CM000663.1:g.241672224G=	GRCh37
NC_000001.9:g.239738847G=	NCBI36
NG_012338.1:g.15831C= , LRG_504:g.15831C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1059-139C=
ENST00000682162.1:c.585-139C=	ENSP00000508203.1:n.585-139C=
ENST00000682567.1:n.633-139C=
ENST00000683521.1:c.556-139C=	ENSP00000506864.1:n.556-139C=
ENST00000684161.1:n.1632C=
ENST00000684483.1:c.556-164C=	ENSP00000507894.1:n.556-164C=
ENST00000366560.4:c.556-139C= MANE Select	ENSP00000355518.4:n.556-139C=
ENST00000366560.3:c.556-139C=	ENSP00000355518.3:n.556-139C=
NM_000143.3:c.556-139C= , LRG_504t1:c.556-139C=	NP_000134.2:n.556-139C=
XM_011544132.1:c.328-139C=	XP_011542434.1:n.328-139C=
XM_011544132.2:c.328-139C=	XP_011542434.1:n.328-139C=
NM_000143.4:c.556-139C= MANE Select	NP_000134.2:n.556-139C=