Canonical Allele Identifier: CA1471368553

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286516A= , CM000666.2:g.80286516A=	GRCh38
NC_000004.11:g.81207670A= , CM000666.1:g.81207670A=	GRCh37
NC_000004.10:g.81426694A=	NCBI36
NG_029501.1:g.24929A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.651A= MANE Select	ENSP00000311697.7:p.Pro217=
ENST00000312465.11:c.651A=	ENSP00000311697.7:p.Pro217=
ENST00000456523.3:c.*175A=	ENSP00000398353.3:n.*175A=
ENST00000503413.1:n.600A=
ENST00000507780.1:c.342+11504A=	ENSP00000423903.1:n.342+11504A=
NM_001291812.1:c.222A=	NP_001278741.1:p.Pro74=
NM_004464.3:c.651A=	NP_004455.2:p.Pro217=
NM_033143.2:c.*175A=	NP_149134.1:n.*175A=
NM_001291812.2:c.222A=	NP_001278741.1:p.Pro74=
NM_004464.4:c.651A= MANE Select	NP_004455.2:p.Pro217=