Canonical Allele Identifier: CA1471368587

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286531G= , CM000666.2:g.80286531G=	GRCh38
NC_000004.11:g.81207685G= , CM000666.1:g.81207685G=	GRCh37
NC_000004.10:g.81426709G=	NCBI36
NG_029501.1:g.24944G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.666G= MANE Select	ENSP00000311697.7:p.Ser222=
ENST00000312465.11:c.666G=	ENSP00000311697.7:p.Ser222=
ENST00000456523.3:c.*190G=	ENSP00000398353.3:n.*190G=
ENST00000503413.1:n.615G=
ENST00000507780.1:c.342+11519G=	ENSP00000423903.1:n.342+11519G=
NM_001291812.1:c.237G=	NP_001278741.1:p.Ser79=
NM_004464.3:c.666G=	NP_004455.2:p.Ser222=
NM_033143.2:c.*190G=	NP_149134.1:n.*190G=
NM_001291812.2:c.237G=	NP_001278741.1:p.Ser79=
NM_004464.4:c.666G= MANE Select	NP_004455.2:p.Ser222=