Canonical Allele Identifier: CA345437297

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241665765A>C (hg19) ; chr1:g.241502465A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502465A>C , CM000663.2:g.241502465A>C	GRCh38
NC_000001.10:g.241665765A>C , CM000663.1:g.241665765A>C	GRCh37
NC_000001.9:g.239732388A>C	NCBI36
NG_012338.1:g.22290T>G , LRG_504:g.22290T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1717T>G
ENST00000682162.1:c.1243T>G	ENSP00000508203.1:n.1243T>G
ENST00000682567.1:n.2762T>G
ENST00000683521.1:c.1214T>G	ENSP00000506864.1:p.Leu405Trp
ENST00000684161.1:n.2429T>G
ENST00000684483.1:c.*610T>G	ENSP00000507894.1:n.*610T>G
ENST00000366560.4:c.1214T>G MANE Select	ENSP00000355518.4:p.Leu405Trp
ENST00000366560.3:c.1214T>G	ENSP00000355518.3:p.Leu405Trp
NM_000143.3:c.1214T>G , LRG_504t1:c.1214T>G	NP_000134.2:p.Leu405Trp
XM_011544132.1:c.986T>G	XP_011542434.1:p.Leu329Trp
XM_011544132.2:c.986T>G	XP_011542434.1:p.Leu329Trp
NM_000143.4:c.1214T>G MANE Select	NP_000134.2:p.Leu405Trp