Canonical Allele Identifier: CA1471368382

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286401A= , CM000666.2:g.80286401A=	GRCh38
NC_000004.11:g.81207555A= , CM000666.1:g.81207555A=	GRCh37
NC_000004.10:g.81426579A=	NCBI36
NG_029501.1:g.24814A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.536A= MANE Select	ENSP00000311697.7:p.His179=
ENST00000312465.11:c.536A=	ENSP00000311697.7:p.His179=
ENST00000456523.3:c.*60A=	ENSP00000398353.3:n.*60A=
ENST00000503413.1:n.485A=
ENST00000507780.1:c.342+11389A=	ENSP00000423903.1:n.342+11389A=
NM_001291812.1:c.107A=	NP_001278741.1:p.His36=
NM_004464.3:c.536A=	NP_004455.2:p.His179=
NM_033143.2:c.*60A=	NP_149134.1:n.*60A=
NM_001291812.2:c.107A=	NP_001278741.1:p.His36=
NM_004464.4:c.536A= MANE Select	NP_004455.2:p.His179=