Canonical Allele Identifier: CA1471368845
Gene: FGF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80286756G= , CM000666.2:g.80286756G= GRCh38
NC_000004.11:g.81207910G= , CM000666.1:g.81207910G= GRCh37
NC_000004.10:g.81426934G= NCBI36
NG_029501.1:g.25169G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000312465.12:c.*84G= MANE Select ENSP00000311697.7:n.*84G=
ENST00000312465.11:c.*84G= ENSP00000311697.7:n.*84G=
ENST00000456523.3:c.*415G= ENSP00000398353.3:n.*415G=
ENST00000503413.1:n.840G=
ENST00000507780.1:c.342+11744G= ENSP00000423903.1:n.342+11744G=
NM_001291812.1:c.*84G= NP_001278741.1:n.*84G=
NM_004464.3:c.*84G= NP_004455.2:n.*84G=
NM_033143.2:c.*415G= NP_149134.1:n.*415G=
NM_001291812.2:c.*84G= NP_001278741.1:n.*84G=
NM_004464.4:c.*84G= MANE Select NP_004455.2:n.*84G=