Canonical Allele Identifier: CA345437327

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241665772A>T (hg19) ; chr1:g.241502472A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502472A>T , CM000663.2:g.241502472A>T	GRCh38
NC_000001.10:g.241665772A>T , CM000663.1:g.241665772A>T	GRCh37
NC_000001.9:g.239732395A>T	NCBI36
NG_012338.1:g.22283T>A , LRG_504:g.22283T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1710T>A
ENST00000682162.1:c.1236T>A	ENSP00000508203.1:n.1236T>A
ENST00000682567.1:n.2755T>A
ENST00000683521.1:c.1207T>A	ENSP00000506864.1:p.Phe403Ile
ENST00000684161.1:n.2422T>A
ENST00000684483.1:c.*603T>A	ENSP00000507894.1:n.*603T>A
ENST00000366560.4:c.1207T>A MANE Select	ENSP00000355518.4:p.Phe403Ile
ENST00000366560.3:c.1207T>A	ENSP00000355518.3:p.Phe403Ile
NM_000143.3:c.1207T>A , LRG_504t1:c.1207T>A	NP_000134.2:p.Phe403Ile
XM_011544132.1:c.979T>A	XP_011542434.1:p.Phe327Ile
XM_011544132.2:c.979T>A	XP_011542434.1:p.Phe327Ile
NM_000143.4:c.1207T>A MANE Select	NP_000134.2:p.Phe403Ile