Canonical Allele Identifier: CA393619986

Gene: FAH

Linked Data

• MyVariant Identifiers: chr15:g.80460611C>A (hg19) ; chr15:g.80168269C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80168269C>A , CM000677.2:g.80168269C>A	GRCh38
NC_000015.9:g.80460611C>A , CM000677.1:g.80460611C>A	GRCh37
NC_000015.8:g.78247666C>A	NCBI36
NG_012833.1:g.20271C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682012.1:n.748C>A
ENST00000684569.1:n.604C>A
ENST00000561421.6:c.559C>A MANE Select	ENSP00000453347.2:p.Pro187Thr
ENST00000646551.1:n.2186C>A
ENST00000261755.9:c.559C>A	ENSP00000261755.5:p.Pro187Thr
ENST00000407106.5:c.559C>A	ENSP00000385080.1:p.Pro187Thr
ENST00000539156.5:c.349C>A	ENSP00000454271.1:p.Pro117Thr
ENST00000558514.1:n.105C>A
ENST00000558627.1:n.487C>A
ENST00000561421.5:c.559C>A	ENSP00000453347.1:p.Pro187Thr
NM_000137.2:c.559C>A	NP_000128.1:p.Pro187Thr
XM_024449872.1:c.559C>A	XP_024305640.1:p.Pro187Thr
NM_000137.4:c.559C>A MANE Select	NP_000128.1:p.Pro187Thr
NM_001374377.1:c.559C>A	NP_001361306.1:p.Pro187Thr
NM_001374380.1:c.559C>A	NP_001361309.1:p.Pro187Thr