Canonical Allele Identifier: CA393620424
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80172157T>G , CM000677.2:g.80172157T>G GRCh38
NC_000015.9:g.80464499T>G , CM000677.1:g.80464499T>G GRCh37
NC_000015.8:g.78251554T>G NCBI36
NG_012833.1:g.24159T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682012.1:n.796-857T>G
ENST00000561421.6:c.615T>G MANE Select ENSP00000453347.2:p.Phe205Leu
ENST00000646551.1:n.2234-5T>G
ENST00000261755.9:c.615T>G ENSP00000261755.5:p.Phe205Leu
ENST00000407106.5:c.615T>G ENSP00000385080.1:p.Phe205Leu
ENST00000539156.5:c.405T>G ENSP00000454271.1:p.Phe135Leu
ENST00000558627.1:n.543T>G
ENST00000561421.5:c.615T>G ENSP00000453347.1:p.Phe205Leu
NM_000137.2:c.615T>G NP_000128.1:p.Phe205Leu
XM_024449872.1:c.615T>G XP_024305640.1:p.Phe205Leu
NM_000137.4:c.615T>G MANE Select NP_000128.1:p.Phe205Leu
NM_001374377.1:c.615T>G NP_001361306.1:p.Phe205Leu
NM_001374380.1:c.615T>G NP_001361309.1:p.Phe205Leu