Canonical Allele Identifier: CA1471368666

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286578A= , CM000666.2:g.80286578A=	GRCh38
NC_000004.11:g.81207732A= , CM000666.1:g.81207732A=	GRCh37
NC_000004.10:g.81426756A=	NCBI36
NG_029501.1:g.24991A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.713A= MANE Select	ENSP00000311697.7:p.Lys238=
ENST00000312465.11:c.713A=	ENSP00000311697.7:p.Lys238=
ENST00000456523.3:c.*237A=	ENSP00000398353.3:n.*237A=
ENST00000503413.1:n.662A=
ENST00000507780.1:c.342+11566A=	ENSP00000423903.1:n.342+11566A=
NM_001291812.1:c.284A=	NP_001278741.1:p.Lys95=
NM_004464.3:c.713A=	NP_004455.2:p.Lys238=
NM_033143.2:c.*237A=	NP_149134.1:n.*237A=
NM_001291812.2:c.284A=	NP_001278741.1:p.Lys95=
NM_004464.4:c.713A= MANE Select	NP_004455.2:p.Lys238=