Canonical Allele Identifier: CA1471368448
Gene: FGF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80286446A= , CM000666.2:g.80286446A= GRCh38
NC_000004.11:g.81207600A= , CM000666.1:g.81207600A= GRCh37
NC_000004.10:g.81426624A= NCBI36
NG_029501.1:g.24859A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000312465.12:c.581A= MANE Select ENSP00000311697.7:p.Lys194=
ENST00000312465.11:c.581A= ENSP00000311697.7:p.Lys194=
ENST00000456523.3:c.*105A= ENSP00000398353.3:n.*105A=
ENST00000503413.1:n.530A=
ENST00000507780.1:c.342+11434A= ENSP00000423903.1:n.342+11434A=
NM_001291812.1:c.152A= NP_001278741.1:p.Lys51=
NM_004464.3:c.581A= NP_004455.2:p.Lys194=
NM_033143.2:c.*105A= NP_149134.1:n.*105A=
NM_001291812.2:c.152A= NP_001278741.1:p.Lys51=
NM_004464.4:c.581A= MANE Select NP_004455.2:p.Lys194=