Canonical Allele Identifier: CA1471368703

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286619C= , CM000666.2:g.80286619C=	GRCh38
NC_000004.11:g.81207773C= , CM000666.1:g.81207773C=	GRCh37
NC_000004.10:g.81426797C=	NCBI36
NG_029501.1:g.25032C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.754C= MANE Select	ENSP00000311697.7:p.Pro252=
ENST00000312465.11:c.754C=	ENSP00000311697.7:p.Pro252=
ENST00000456523.3:c.*278C=	ENSP00000398353.3:n.*278C=
ENST00000503413.1:n.703C=
ENST00000507780.1:c.342+11607C=	ENSP00000423903.1:n.342+11607C=
NM_001291812.1:c.325C=	NP_001278741.1:p.Pro109=
NM_004464.3:c.754C=	NP_004455.2:p.Pro252=
NM_033143.2:c.*278C=	NP_149134.1:n.*278C=
NM_001291812.2:c.325C=	NP_001278741.1:p.Pro109=
NM_004464.4:c.754C= MANE Select	NP_004455.2:p.Pro252=