Canonical Allele Identifier: CA1471368466

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286464G= , CM000666.2:g.80286464G=	GRCh38
NC_000004.11:g.81207618G= , CM000666.1:g.81207618G=	GRCh37
NC_000004.10:g.81426642G=	NCBI36
NG_029501.1:g.24877G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.599G= MANE Select	ENSP00000311697.7:p.Arg200=
ENST00000312465.11:c.599G=	ENSP00000311697.7:p.Arg200=
ENST00000456523.3:c.*123G=	ENSP00000398353.3:n.*123G=
ENST00000503413.1:n.548G=
ENST00000507780.1:c.342+11452G=	ENSP00000423903.1:n.342+11452G=
NM_001291812.1:c.170G=	NP_001278741.1:p.Arg57=
NM_004464.3:c.599G=	NP_004455.2:p.Arg200=
NM_033143.2:c.*123G=	NP_149134.1:n.*123G=
NM_001291812.2:c.170G=	NP_001278741.1:p.Arg57=
NM_004464.4:c.599G= MANE Select	NP_004455.2:p.Arg200=