Canonical Allele Identifier: CA393620001
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80168276T>C , CM000677.2:g.80168276T>C GRCh38
NC_000015.9:g.80460618T>C , CM000677.1:g.80460618T>C GRCh37
NC_000015.8:g.78247673T>C NCBI36
NG_012833.1:g.20278T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682012.1:n.755T>C
ENST00000684569.1:n.611T>C
ENST00000561421.6:c.566T>C MANE Select ENSP00000453347.2:p.Val189Ala
ENST00000646551.1:n.2193T>C
ENST00000261755.9:c.566T>C ENSP00000261755.5:p.Val189Ala
ENST00000407106.5:c.566T>C ENSP00000385080.1:p.Val189Ala
ENST00000539156.5:c.356T>C ENSP00000454271.1:p.Val119Ala
ENST00000558514.1:n.112T>C
ENST00000558627.1:n.494T>C
ENST00000561421.5:c.566T>C ENSP00000453347.1:p.Val189Ala
NM_000137.2:c.566T>C NP_000128.1:p.Val189Ala
XM_024449872.1:c.566T>C XP_024305640.1:p.Val189Ala
NM_000137.4:c.566T>C MANE Select NP_000128.1:p.Val189Ala
NM_001374377.1:c.566T>C NP_001361306.1:p.Val189Ala
NM_001374380.1:c.566T>C NP_001361309.1:p.Val189Ala