Canonical Allele Identifier: CA357397438
Gene: FGF5 HGNC NCBI

Linked Data

dbSNP Id: rs1720721501
gnomAD v4: 4-80286418-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80286418G>A , CM000666.2:g.80286418G>A GRCh38
NC_000004.11:g.81207572G>A , CM000666.1:g.81207572G>A GRCh37
NC_000004.10:g.81426596G>A NCBI36
NG_029501.1:g.24831G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000312465.12:c.553G>A MANE Select ENSP00000311697.7:p.Gly185Arg
ENST00000312465.11:c.553G>A ENSP00000311697.7:p.Gly185Arg
ENST00000456523.3:c.*77G>A ENSP00000398353.3:n.*77G>A
ENST00000503413.1:n.502G>A
ENST00000507780.1:c.342+11406G>A ENSP00000423903.1:n.342+11406G>A
NM_001291812.1:c.124G>A NP_001278741.1:p.Gly42Arg
NM_004464.3:c.553G>A NP_004455.2:p.Gly185Arg
NM_033143.2:c.*77G>A NP_149134.1:n.*77G>A
NM_001291812.2:c.124G>A NP_001278741.1:p.Gly42Arg
NM_004464.4:c.553G>A MANE Select NP_004455.2:p.Gly185Arg