Canonical Allele Identifier: CA1471368349

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286385T= , CM000666.2:g.80286385T=	GRCh38
NC_000004.11:g.81207539T= , CM000666.1:g.81207539T=	GRCh37
NC_000004.10:g.81426563T=	NCBI36
NG_029501.1:g.24798T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.520T= MANE Select	ENSP00000311697.7:p.Tyr174=
ENST00000312465.11:c.520T=	ENSP00000311697.7:p.Tyr174=
ENST00000456523.3:c.*44T=	ENSP00000398353.3:n.*44T=
ENST00000503413.1:n.469T=
ENST00000507780.1:c.342+11373T=	ENSP00000423903.1:n.342+11373T=
NM_001291812.1:c.91T=	NP_001278741.1:p.Tyr31=
NM_004464.3:c.520T=	NP_004455.2:p.Tyr174=
NM_033143.2:c.*44T=	NP_149134.1:n.*44T=
NM_001291812.2:c.91T=	NP_001278741.1:p.Tyr31=
NM_004464.4:c.520T= MANE Select	NP_004455.2:p.Tyr174=