Canonical Allele Identifier: CA345437479

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241665819A>T (hg19) ; chr1:g.241502519A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502519A>T , CM000663.2:g.241502519A>T	GRCh38
NC_000001.10:g.241665819A>T , CM000663.1:g.241665819A>T	GRCh37
NC_000001.9:g.239732442A>T	NCBI36
NG_012338.1:g.22236T>A , LRG_504:g.22236T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1663T>A
ENST00000682162.1:c.1189T>A	ENSP00000508203.1:n.1189T>A
ENST00000682567.1:n.2708T>A
ENST00000683521.1:c.1160T>A	ENSP00000506864.1:p.Val387Asp
ENST00000684161.1:n.2375T>A
ENST00000684483.1:c.*556T>A	ENSP00000507894.1:n.*556T>A
ENST00000366560.4:c.1160T>A MANE Select	ENSP00000355518.4:p.Val387Asp
ENST00000366560.3:c.1160T>A	ENSP00000355518.3:p.Val387Asp
NM_000143.3:c.1160T>A , LRG_504t1:c.1160T>A	NP_000134.2:p.Val387Asp
XM_011544132.1:c.932T>A	XP_011542434.1:p.Val311Asp
XM_011544132.2:c.932T>A	XP_011542434.1:p.Val311Asp
NM_000143.4:c.1160T>A MANE Select	NP_000134.2:p.Val387Asp