Canonical Allele Identifier: CA393619498

Gene: FAH

Linked Data

• MyVariant Identifiers: chr15:g.80454675A>T (hg19) ; chr15:g.80162333A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80162333A>T , CM000677.2:g.80162333A>T	GRCh38
NC_000015.9:g.80454675A>T , CM000677.1:g.80454675A>T	GRCh37
NC_000015.8:g.78241730A>T	NCBI36
NG_012833.1:g.14335A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.452A>T	ENSP00000507680.1:p.Asn151Ile
ENST00000682012.1:n.527A>T
ENST00000683593.1:n.2115A>T
ENST00000684363.1:c.365-59A>T	ENSP00000507314.1:n.365-59A>T
ENST00000684569.1:n.497A>T
ENST00000561421.6:c.452A>T MANE Select	ENSP00000453347.2:p.Asn151Ile
ENST00000646551.1:n.1939A>T
ENST00000261755.9:c.452A>T	ENSP00000261755.5:p.Asn151Ile
ENST00000407106.5:c.452A>T	ENSP00000385080.1:p.Asn151Ile
ENST00000537726.5:n.598A>T
ENST00000539156.5:c.242A>T	ENSP00000454271.1:p.Asn81Ile
ENST00000558022.5:c.452A>T	ENSP00000453152.1:p.Asn151Ile
ENST00000558627.1:n.380A>T
ENST00000558767.5:n.713A>T
ENST00000561369.1:n.596A>T
ENST00000561421.5:c.452A>T	ENSP00000453347.1:p.Asn151Ile
NM_000137.2:c.452A>T	NP_000128.1:p.Asn151Ile
XM_024449872.1:c.452A>T	XP_024305640.1:p.Asn151Ile
NM_000137.4:c.452A>T MANE Select	NP_000128.1:p.Asn151Ile
NM_001374377.1:c.452A>T	NP_001361306.1:p.Asn151Ile
NM_001374380.1:c.452A>T	NP_001361309.1:p.Asn151Ile