Canonical Allele Identifier: CA2742041098

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80153170_80153171delinsAG , CM000677.2:g.80153170_80153171delinsAG	GRCh38
NC_000015.9:g.80445512_80445513delinsAG , CM000677.1:g.80445512_80445513delinsAG	GRCh37
NC_000015.8:g.78232567_78232568delinsAG	NCBI36
NG_012833.1:g.5172_5173delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.81+35_81+36delinsAG	ENSP00000507680.1:n.81+35_81+36delinsAG
ENST00000682012.1:n.156+35_156+36delinsAG
ENST00000684363.1:c.81+35_81+36delinsAG	ENSP00000507314.1:n.81+35_81+36delinsAG
ENST00000684569.1:n.126+35_126+36delinsAG
ENST00000561421.6:c.81+35_81+36delinsAG MANE Select	ENSP00000453347.2:n.81+35_81+36delinsAG
ENST00000261755.9:c.81+35_81+36delinsAG	ENSP00000261755.5:n.81+35_81+36delinsAG
ENST00000407106.5:c.81+35_81+36delinsAG	ENSP00000385080.1:n.81+35_81+36delinsAG
ENST00000537726.5:n.163+35_163+36delinsAG
ENST00000558022.5:c.81+35_81+36delinsAG	ENSP00000453152.1:n.81+35_81+36delinsAG
ENST00000558767.5:n.342+35_342+36delinsAG
ENST00000561369.1:n.161+35_161+36delinsAG
ENST00000561421.5:c.81+35_81+36delinsAG	ENSP00000453347.1:n.81+35_81+36delinsAG
NM_000137.2:c.81+35_81+36delinsAG	NP_000128.1:n.81+35_81+36delinsAG
XM_024449872.1:c.81+35_81+36delinsAG	XP_024305640.1:n.81+35_81+36delinsAG
NM_000137.4:c.81+35_81+36delinsAG MANE Select	NP_000128.1:n.81+35_81+36delinsAG
NM_001374377.1:c.81+35_81+36delinsAG	NP_001361306.1:n.81+35_81+36delinsAG
NM_001374380.1:c.81+35_81+36delinsAG	NP_001361309.1:n.81+35_81+36delinsAG