Canonical Allele Identifier: CA2539147781

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152959_80152970del , CM000677.2:g.80152959_80152970del	GRCh38
NC_000015.9:g.80445301_80445312del , CM000677.1:g.80445301_80445312del	GRCh37
NC_000015.8:g.78232356_78232367del	NCBI36
NG_012833.1:g.4961_4972del

Transcript Alleles

HGVS	Amino-acid change
ENST00000558767.6:c.-96_-85del	ENSP00000507680.1:n.-96_-85del
ENST00000261755.9:c.-29-67_-29-56del	ENSP00000261755.5:n.-29-67_-29-56del
ENST00000407106.5:c.-30+54_-29-56del	ENSP00000385080.1:n.-30+54_-29-56del
ENST00000537726.5:n.54-67_54-56del
ENST00000558022.5:c.-29-67_-29-56del	ENSP00000453152.1:n.-29-67_-29-56del
ENST00000558767.5:n.166_177del
ENST00000561369.1:n.51+54_52-56del
ENST00000561421.5:c.-96_-85del	ENSP00000453347.1:n.-96_-85del
NM_000137.2:c.-96_-85del	NP_000128.1:n.-96_-85del
XM_024449872.1:c.-30+54_-29-56del	XP_024305640.1:n.-30+54_-29-56del
NM_001374377.1:c.-30+54_-29-56del	NP_001361306.1:n.-30+54_-29-56del
NM_001374380.1:c.-29-67_-29-56del	NP_001361309.1:n.-29-67_-29-56del