Canonical Allele Identifier: CA424075797

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241667439C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504139C>T , CM000663.2:g.241504139C>T	GRCh38
NC_000001.10:g.241667439C>T , CM000663.1:g.241667439C>T	GRCh37
NC_000001.9:g.239734062C>T	NCBI36
NG_012338.1:g.20616G>A , LRG_504:g.20616G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1514G>A
ENST00000682162.1:c.1040G>A	ENSP00000508203.1:n.1040G>A
ENST00000682567.1:n.1088G>A
ENST00000683521.1:c.1011G>A	ENSP00000506864.1:p.Lys337=
ENST00000684161.1:n.2226G>A
ENST00000684483.1:c.*407G>A	ENSP00000507894.1:n.*407G>A
ENST00000366560.4:c.1011G>A MANE Select	ENSP00000355518.4:p.Lys337=
ENST00000366560.3:c.1011G>A	ENSP00000355518.3:p.Lys337=
NM_000143.3:c.1011G>A , LRG_504t1:c.1011G>A	NP_000134.2:p.Lys337=
XM_011544132.1:c.783G>A	XP_011542434.1:p.Lys261=
XM_011544132.2:c.783G>A	XP_011542434.1:p.Lys261=
NM_000143.4:c.1011G>A MANE Select	NP_000134.2:p.Lys337=