Canonical Allele Identifier: CA424075795

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241667436T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504136T>A , CM000663.2:g.241504136T>A	GRCh38
NC_000001.10:g.241667436T>A , CM000663.1:g.241667436T>A	GRCh37
NC_000001.9:g.239734059T>A	NCBI36
NG_012338.1:g.20619A>T , LRG_504:g.20619A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1517A>T
ENST00000682162.1:c.1043A>T	ENSP00000508203.1:n.1043A>T
ENST00000682567.1:n.1091A>T
ENST00000683521.1:c.1014A>T	ENSP00000506864.1:p.Ile338=
ENST00000684161.1:n.2229A>T
ENST00000684483.1:c.*410A>T	ENSP00000507894.1:n.*410A>T
ENST00000366560.4:c.1014A>T MANE Select	ENSP00000355518.4:p.Ile338=
ENST00000366560.3:c.1014A>T	ENSP00000355518.3:p.Ile338=
NM_000143.3:c.1014A>T , LRG_504t1:c.1014A>T	NP_000134.2:p.Ile338=
XM_011544132.1:c.786A>T	XP_011542434.1:p.Ile262=
XM_011544132.2:c.786A>T	XP_011542434.1:p.Ile262=
NM_000143.4:c.1014A>T MANE Select	NP_000134.2:p.Ile338=