Canonical Allele Identifier: CA2748368434

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512318_241512319insATA , CM000663.2:g.241512318_241512319insATA	GRCh38
NC_000001.10:g.241675618_241675619insATA , CM000663.1:g.241675618_241675619insATA	GRCh37
NC_000001.9:g.239742241_239742242insATA	NCBI36
NG_012338.1:g.12436_12437insTAT , LRG_504:g.12436_12437insTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.882-176_882-175insTAT
ENST00000682162.1:c.408-176_408-175insTAT	ENSP00000508203.1:n.408-176_408-175insTAT
ENST00000682567.1:n.456-176_456-175insTAT
ENST00000683521.1:c.379-176_379-175insTAT	ENSP00000506864.1:n.379-176_379-175insTAT
ENST00000684483.1:c.379-176_379-175insTAT	ENSP00000507894.1:n.379-176_379-175insTAT
ENST00000366560.4:c.379-176_379-175insTAT MANE Select	ENSP00000355518.4:n.379-176_379-175insTAT
ENST00000366560.3:c.379-176_379-175insTAT	ENSP00000355518.3:n.379-176_379-175insTAT
ENST00000497042.1:n.75-176_75-175insTAT
NM_000143.3:c.379-176_379-175insTAT , LRG_504t1:c.379-176_379-175insTAT	NP_000134.2:n.379-176_379-175insTAT
XM_011544132.1:c.151-176_151-175insTAT	XP_011542434.1:n.151-176_151-175insTAT
XM_011544132.2:c.151-176_151-175insTAT	XP_011542434.1:n.151-176_151-175insTAT
NM_000143.4:c.379-176_379-175insTAT MANE Select	NP_000134.2:n.379-176_379-175insTAT