Canonical Allele Identifier: CA1471368356

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286387T= , CM000666.2:g.80286387T=	GRCh38
NC_000004.11:g.81207541T= , CM000666.1:g.81207541T=	GRCh37
NC_000004.10:g.81426565T=	NCBI36
NG_029501.1:g.24800T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.522T= MANE Select	ENSP00000311697.7:p.Tyr174=
ENST00000312465.11:c.522T=	ENSP00000311697.7:p.Tyr174=
ENST00000456523.3:c.*46T=	ENSP00000398353.3:n.*46T=
ENST00000503413.1:n.471T=
ENST00000507780.1:c.342+11375T=	ENSP00000423903.1:n.342+11375T=
NM_001291812.1:c.93T=	NP_001278741.1:p.Tyr31=
NM_004464.3:c.522T=	NP_004455.2:p.Tyr174=
NM_033143.2:c.*46T=	NP_149134.1:n.*46T=
NM_001291812.2:c.93T=	NP_001278741.1:p.Tyr31=
NM_004464.4:c.522T= MANE Select	NP_004455.2:p.Tyr174=