Canonical Allele Identifier: CA1471368398

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286411A= , CM000666.2:g.80286411A=	GRCh38
NC_000004.11:g.81207565A= , CM000666.1:g.81207565A=	GRCh37
NC_000004.10:g.81426589A=	NCBI36
NG_029501.1:g.24824A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.546A= MANE Select	ENSP00000311697.7:p.Glu182=
ENST00000312465.11:c.546A=	ENSP00000311697.7:p.Glu182=
ENST00000456523.3:c.*70A=	ENSP00000398353.3:n.*70A=
ENST00000503413.1:n.495A=
ENST00000507780.1:c.342+11399A=	ENSP00000423903.1:n.342+11399A=
NM_001291812.1:c.117A=	NP_001278741.1:p.Glu39=
NM_004464.3:c.546A=	NP_004455.2:p.Glu182=
NM_033143.2:c.*70A=	NP_149134.1:n.*70A=
NM_001291812.2:c.117A=	NP_001278741.1:p.Glu39=
NM_004464.4:c.546A= MANE Select	NP_004455.2:p.Glu182=