Canonical Allele Identifier: CA1471368411

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286421C= , CM000666.2:g.80286421C=	GRCh38
NC_000004.11:g.81207575C= , CM000666.1:g.81207575C=	GRCh37
NC_000004.10:g.81426599C=	NCBI36
NG_029501.1:g.24834C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.556C= MANE Select	ENSP00000311697.7:p.Arg186=
ENST00000312465.11:c.556C=	ENSP00000311697.7:p.Arg186=
ENST00000456523.3:c.*80C=	ENSP00000398353.3:n.*80C=
ENST00000503413.1:n.505C=
ENST00000507780.1:c.342+11409C=	ENSP00000423903.1:n.342+11409C=
NM_001291812.1:c.127C=	NP_001278741.1:p.Arg43=
NM_004464.3:c.556C=	NP_004455.2:p.Arg186=
NM_033143.2:c.*80C=	NP_149134.1:n.*80C=
NM_001291812.2:c.127C=	NP_001278741.1:p.Arg43=
NM_004464.4:c.556C= MANE Select	NP_004455.2:p.Arg186=