Canonical Allele Identifier: CA1471368367

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286393A= , CM000666.2:g.80286393A=	GRCh38
NC_000004.11:g.81207547A= , CM000666.1:g.81207547A=	GRCh37
NC_000004.10:g.81426571A=	NCBI36
NG_029501.1:g.24806A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.528A= MANE Select	ENSP00000311697.7:p.Ser176=
ENST00000312465.11:c.528A=	ENSP00000311697.7:p.Ser176=
ENST00000456523.3:c.*52A=	ENSP00000398353.3:n.*52A=
ENST00000503413.1:n.477A=
ENST00000507780.1:c.342+11381A=	ENSP00000423903.1:n.342+11381A=
NM_001291812.1:c.99A=	NP_001278741.1:p.Ser33=
NM_004464.3:c.528A=	NP_004455.2:p.Ser176=
NM_033143.2:c.*52A=	NP_149134.1:n.*52A=
NM_001291812.2:c.99A=	NP_001278741.1:p.Ser33=
NM_004464.4:c.528A= MANE Select	NP_004455.2:p.Ser176=