Canonical Allele Identifier: CA1471368328

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286372T= , CM000666.2:g.80286372T=	GRCh38
NC_000004.11:g.81207526T= , CM000666.1:g.81207526T=	GRCh37
NC_000004.10:g.81426550T=	NCBI36
NG_029501.1:g.24785T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.507T= MANE Select	ENSP00000311697.7:p.Asn169=
ENST00000312465.11:c.507T=	ENSP00000311697.7:p.Asn169=
ENST00000456523.3:c.*31T=	ENSP00000398353.3:n.*31T=
ENST00000503413.1:n.456T=
ENST00000507780.1:c.342+11360T=	ENSP00000423903.1:n.342+11360T=
NM_001291812.1:c.78T=	NP_001278741.1:p.Asn26=
NM_004464.3:c.507T=	NP_004455.2:p.Asn169=
NM_033143.2:c.*31T=	NP_149134.1:n.*31T=
NM_001291812.2:c.78T=	NP_001278741.1:p.Asn26=
NM_004464.4:c.507T= MANE Select	NP_004455.2:p.Asn169=