Canonical Allele Identifier: CA1471368431

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286428G= , CM000666.2:g.80286428G=	GRCh38
NC_000004.11:g.81207582G= , CM000666.1:g.81207582G=	GRCh37
NC_000004.10:g.81426606G=	NCBI36
NG_029501.1:g.24841G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.563G= MANE Select	ENSP00000311697.7:p.Trp188=
ENST00000312465.11:c.563G=	ENSP00000311697.7:p.Trp188=
ENST00000456523.3:c.*87G=	ENSP00000398353.3:n.*87G=
ENST00000503413.1:n.512G=
ENST00000507780.1:c.342+11416G=	ENSP00000423903.1:n.342+11416G=
NM_001291812.1:c.134G=	NP_001278741.1:p.Trp45=
NM_004464.3:c.563G=	NP_004455.2:p.Trp188=
NM_033143.2:c.*87G=	NP_149134.1:n.*87G=
NM_001291812.2:c.134G=	NP_001278741.1:p.Trp45=
NM_004464.4:c.563G= MANE Select	NP_004455.2:p.Trp188=