Canonical Allele Identifier: CA1471368889
Gene: FGF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80286799A= , CM000666.2:g.80286799A= GRCh38
NC_000004.11:g.81207953A= , CM000666.1:g.81207953A= GRCh37
NC_000004.10:g.81426977A= NCBI36
NG_029501.1:g.25212A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000312465.12:c.*127A= MANE Select ENSP00000311697.7:n.*127A=
ENST00000312465.11:c.*127A= ENSP00000311697.7:n.*127A=
ENST00000456523.3:c.*458A= ENSP00000398353.3:n.*458A=
ENST00000503413.1:n.883A=
ENST00000507780.1:c.342+11787A= ENSP00000423903.1:n.342+11787A=
NM_001291812.1:c.*127A= NP_001278741.1:n.*127A=
NM_004464.3:c.*127A= NP_004455.2:n.*127A=
NM_033143.2:c.*458A= NP_149134.1:n.*458A=
NM_001291812.2:c.*127A= NP_001278741.1:n.*127A=
NM_004464.4:c.*127A= MANE Select NP_004455.2:n.*127A=