Canonical Allele Identifier: CA2629875847

Gene: FAH

Linked Data

• gnomAD v4: 15-80168400-GCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80168401_80168402del , CM000677.2:g.80168401_80168402del	GRCh38
NC_000015.9:g.80460743_80460744del , CM000677.1:g.80460743_80460744del	GRCh37
NC_000015.8:g.78247798_78247799del	NCBI36
NG_012833.1:g.20403_20404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.795+85_795+86del
ENST00000684569.1:n.651+85_651+86del
ENST00000561421.6:c.606+85_606+86del MANE Select	ENSP00000453347.2:n.606+85_606+86del
ENST00000646551.1:n.2233+85_2233+86del
ENST00000261755.9:c.606+85_606+86del	ENSP00000261755.5:n.606+85_606+86del
ENST00000407106.5:c.606+85_606+86del	ENSP00000385080.1:n.606+85_606+86del
ENST00000539156.5:c.396+85_396+86del	ENSP00000454271.1:n.396+85_396+86del
ENST00000558514.1:n.237_238del
ENST00000558627.1:n.534+85_534+86del
ENST00000561421.5:c.606+85_606+86del	ENSP00000453347.1:n.606+85_606+86del
NM_000137.2:c.606+85_606+86del	NP_000128.1:n.606+85_606+86del
XM_024449872.1:c.606+85_606+86del	XP_024305640.1:n.606+85_606+86del
NM_000137.4:c.606+85_606+86del MANE Select	NP_000128.1:n.606+85_606+86del
NM_001374377.1:c.606+85_606+86del	NP_001361306.1:n.606+85_606+86del
NM_001374380.1:c.606+85_606+86del	NP_001361309.1:n.606+85_606+86del