Canonical Allele Identifier: CA1471368688
Gene: FGF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80286595A= , CM000666.2:g.80286595A= GRCh38
NC_000004.11:g.81207749A= , CM000666.1:g.81207749A= GRCh37
NC_000004.10:g.81426773A= NCBI36
NG_029501.1:g.25008A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000312465.12:c.730A= MANE Select ENSP00000311697.7:p.Lys244=
ENST00000312465.11:c.730A= ENSP00000311697.7:p.Lys244=
ENST00000456523.3:c.*254A= ENSP00000398353.3:n.*254A=
ENST00000503413.1:n.679A=
ENST00000507780.1:c.342+11583A= ENSP00000423903.1:n.342+11583A=
NM_001291812.1:c.301A= NP_001278741.1:p.Lys101=
NM_004464.3:c.730A= NP_004455.2:p.Lys244=
NM_033143.2:c.*254A= NP_149134.1:n.*254A=
NM_001291812.2:c.301A= NP_001278741.1:p.Lys101=
NM_004464.4:c.730A= MANE Select NP_004455.2:p.Lys244=