Canonical Allele Identifier: CA1471368419

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286425A= , CM000666.2:g.80286425A=	GRCh38
NC_000004.11:g.81207579A= , CM000666.1:g.81207579A=	GRCh37
NC_000004.10:g.81426603A=	NCBI36
NG_029501.1:g.24838A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.560A= MANE Select	ENSP00000311697.7:p.Glu187=
ENST00000312465.11:c.560A=	ENSP00000311697.7:p.Glu187=
ENST00000456523.3:c.*84A=	ENSP00000398353.3:n.*84A=
ENST00000503413.1:n.509A=
ENST00000507780.1:c.342+11413A=	ENSP00000423903.1:n.342+11413A=
NM_001291812.1:c.131A=	NP_001278741.1:p.Glu44=
NM_004464.3:c.560A=	NP_004455.2:p.Glu187=
NM_033143.2:c.*84A=	NP_149134.1:n.*84A=
NM_001291812.2:c.131A=	NP_001278741.1:p.Glu44=
NM_004464.4:c.560A= MANE Select	NP_004455.2:p.Glu187=