Canonical Allele Identifier: CA393620050

Gene: FAH

Linked Data

• MyVariant Identifiers: chr15:g.80460642A>C (hg19) ; chr15:g.80168300A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80168300A>C , CM000677.2:g.80168300A>C	GRCh38
NC_000015.9:g.80460642A>C , CM000677.1:g.80460642A>C	GRCh37
NC_000015.8:g.78247697A>C	NCBI36
NG_012833.1:g.20302A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.779A>C
ENST00000684569.1:n.635A>C
ENST00000561421.6:c.590A>C MANE Select	ENSP00000453347.2:p.Asp197Ala
ENST00000646551.1:n.2217A>C
ENST00000261755.9:c.590A>C	ENSP00000261755.5:p.Asp197Ala
ENST00000407106.5:c.590A>C	ENSP00000385080.1:p.Asp197Ala
ENST00000539156.5:c.380A>C	ENSP00000454271.1:p.Asp127Ala
ENST00000558514.1:n.136A>C
ENST00000558627.1:n.518A>C
ENST00000561421.5:c.590A>C	ENSP00000453347.1:p.Asp197Ala
NM_000137.2:c.590A>C	NP_000128.1:p.Asp197Ala
XM_024449872.1:c.590A>C	XP_024305640.1:p.Asp197Ala
NM_000137.4:c.590A>C MANE Select	NP_000128.1:p.Asp197Ala
NM_001374377.1:c.590A>C	NP_001361306.1:p.Asp197Ala
NM_001374380.1:c.590A>C	NP_001361309.1:p.Asp197Ala