Canonical Allele Identifier: CA345440122

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241675394G>A (hg19) ; chr1:g.241512094G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512094G>A , CM000663.2:g.241512094G>A	GRCh38
NC_000001.10:g.241675394G>A , CM000663.1:g.241675394G>A	GRCh37
NC_000001.9:g.239742017G>A	NCBI36
NG_012338.1:g.12661C>T , LRG_504:g.12661C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.931C>T
ENST00000682162.1:c.457C>T	ENSP00000508203.1:n.457C>T
ENST00000682567.1:n.505C>T
ENST00000683521.1:c.428C>T	ENSP00000506864.1:p.Thr143Ile
ENST00000684483.1:c.428C>T	ENSP00000507894.1:p.Thr143Ile
ENST00000366560.4:c.428C>T MANE Select	ENSP00000355518.4:p.Thr143Ile
ENST00000366560.3:c.428C>T	ENSP00000355518.3:p.Thr143Ile
ENST00000497042.1:n.124C>T
NM_000143.3:c.428C>T , LRG_504t1:c.428C>T	NP_000134.2:p.Thr143Ile
XM_011544132.1:c.200C>T	XP_011542434.1:p.Thr67Ile
XM_011544132.2:c.200C>T	XP_011542434.1:p.Thr67Ile
NM_000143.4:c.428C>T MANE Select	NP_000134.2:p.Thr143Ile