Canonical Allele Identifier: CA1229582120

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512201_241512203delinsCCA , CM000663.2:g.241512201_241512203delinsCCA	GRCh38
NC_000001.10:g.241675501_241675503delinsCCA , CM000663.1:g.241675501_241675503delinsCCA	GRCh37
NC_000001.9:g.239742124_239742126delinsCCA	NCBI36
NG_012338.1:g.12552_12554delinsTGG , LRG_504:g.12552_12554delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.882-60_882-58delinsTGG
ENST00000682162.1:c.408-60_408-58delinsTGG	ENSP00000508203.1:n.408-60_408-58delinsTGG
ENST00000682567.1:n.456-60_456-58delinsTGG
ENST00000683521.1:c.379-60_379-58delinsTGG	ENSP00000506864.1:n.379-60_379-58delinsTGG
ENST00000684483.1:c.379-60_379-58delinsTGG	ENSP00000507894.1:n.379-60_379-58delinsTGG
ENST00000366560.4:c.379-60_379-58delinsTGG MANE Select	ENSP00000355518.4:n.379-60_379-58delinsTGG
ENST00000366560.3:c.379-60_379-58delinsTGG	ENSP00000355518.3:n.379-60_379-58delinsTGG
ENST00000497042.1:n.75-60_75-58delinsTGG
NM_000143.3:c.379-60_379-58delinsTGG , LRG_504t1:c.379-60_379-58delinsTGG	NP_000134.2:n.379-60_379-58delinsTGG
XM_011544132.1:c.151-60_151-58delinsTGG	XP_011542434.1:n.151-60_151-58delinsTGG
XM_011544132.2:c.151-60_151-58delinsTGG	XP_011542434.1:n.151-60_151-58delinsTGG
NM_000143.4:c.379-60_379-58delinsTGG MANE Select	NP_000134.2:n.379-60_379-58delinsTGG