Canonical Allele Identifier: CA1471368362

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286388G= , CM000666.2:g.80286388G=	GRCh38
NC_000004.11:g.81207542G= , CM000666.1:g.81207542G=	GRCh37
NC_000004.10:g.81426566G=	NCBI36
NG_029501.1:g.24801G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.523G= MANE Select	ENSP00000311697.7:p.Ala175=
ENST00000312465.11:c.523G=	ENSP00000311697.7:p.Ala175=
ENST00000456523.3:c.*47G=	ENSP00000398353.3:n.*47G=
ENST00000503413.1:n.472G=
ENST00000507780.1:c.342+11376G=	ENSP00000423903.1:n.342+11376G=
NM_001291812.1:c.94G=	NP_001278741.1:p.Ala32=
NM_004464.3:c.523G=	NP_004455.2:p.Ala175=
NM_033143.2:c.*47G=	NP_149134.1:n.*47G=
NM_001291812.2:c.94G=	NP_001278741.1:p.Ala32=
NM_004464.4:c.523G= MANE Select	NP_004455.2:p.Ala175=