Canonical Allele Identifier: CA393619443

Gene: FAH

Linked Data

• MyVariant Identifiers: chr15:g.80454651A>C (hg19) ; chr15:g.80162309A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80162309A>C , CM000677.2:g.80162309A>C	GRCh38
NC_000015.9:g.80454651A>C , CM000677.1:g.80454651A>C	GRCh37
NC_000015.8:g.78241706A>C	NCBI36
NG_012833.1:g.14311A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.428A>C	ENSP00000507680.1:p.Asp143Ala
ENST00000682012.1:n.503A>C
ENST00000683593.1:n.2091A>C
ENST00000684363.1:c.365-83A>C	ENSP00000507314.1:n.365-83A>C
ENST00000684569.1:n.473A>C
ENST00000561421.6:c.428A>C MANE Select	ENSP00000453347.2:p.Asp143Ala
ENST00000646551.1:n.1915A>C
ENST00000261755.9:c.428A>C	ENSP00000261755.5:p.Asp143Ala
ENST00000407106.5:c.428A>C	ENSP00000385080.1:p.Asp143Ala
ENST00000537726.5:n.574A>C
ENST00000539156.5:c.218A>C	ENSP00000454271.1:p.Asp73Ala
ENST00000558022.5:c.428A>C	ENSP00000453152.1:p.Asp143Ala
ENST00000558627.1:n.356A>C
ENST00000558767.5:n.689A>C
ENST00000561369.1:n.572A>C
ENST00000561421.5:c.428A>C	ENSP00000453347.1:p.Asp143Ala
NM_000137.2:c.428A>C	NP_000128.1:p.Asp143Ala
XM_024449872.1:c.428A>C	XP_024305640.1:p.Asp143Ala
NM_000137.4:c.428A>C MANE Select	NP_000128.1:p.Asp143Ala
NM_001374377.1:c.428A>C	NP_001361306.1:p.Asp143Ala
NM_001374380.1:c.428A>C	NP_001361309.1:p.Asp143Ala