Canonical Allele Identifier: CA2629878151

Gene: FAH

Linked Data

• gnomAD v4: 15-80162183-A-ACAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80162185_80162188dup , CM000677.2:g.80162185_80162188dup	GRCh38
NC_000015.9:g.80454527_80454530dup , CM000677.1:g.80454527_80454530dup	GRCh37
NC_000015.8:g.78241582_78241585dup	NCBI36
NG_012833.1:g.14187_14190dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.365-61_365-58dup	ENSP00000507680.1:n.365-61_365-58dup
ENST00000682012.1:n.440-61_440-58dup
ENST00000683593.1:n.1967_1970dup
ENST00000684363.1:c.365-207_365-204dup	ENSP00000507314.1:n.365-207_365-204dup
ENST00000684569.1:n.410-61_410-58dup
ENST00000561421.6:c.365-61_365-58dup MANE Select	ENSP00000453347.2:n.365-61_365-58dup
ENST00000646551.1:n.1852-61_1852-58dup
ENST00000261755.9:c.365-61_365-58dup	ENSP00000261755.5:n.365-61_365-58dup
ENST00000407106.5:c.365-61_365-58dup	ENSP00000385080.1:n.365-61_365-58dup
ENST00000537726.5:n.511-61_511-58dup
ENST00000539156.5:c.155-61_155-58dup	ENSP00000454271.1:n.155-61_155-58dup
ENST00000558022.5:c.365-61_365-58dup	ENSP00000453152.1:n.365-61_365-58dup
ENST00000558627.1:n.293-61_293-58dup
ENST00000558767.5:n.626-61_626-58dup
ENST00000561369.1:n.509-61_509-58dup
ENST00000561421.5:c.365-61_365-58dup	ENSP00000453347.1:n.365-61_365-58dup
NM_000137.2:c.365-61_365-58dup	NP_000128.1:n.365-61_365-58dup
XM_024449872.1:c.365-61_365-58dup	XP_024305640.1:n.365-61_365-58dup
NM_000137.4:c.365-61_365-58dup MANE Select	NP_000128.1:n.365-61_365-58dup
NM_001374377.1:c.365-61_365-58dup	NP_001361306.1:n.365-61_365-58dup
NM_001374380.1:c.365-61_365-58dup	NP_001361309.1:n.365-61_365-58dup