Canonical Allele Identifier: CA357397617
Gene: FGF5 HGNC NCBI

Linked Data

gnomAD v4: 4-80286445-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80286445A>G , CM000666.2:g.80286445A>G GRCh38
NC_000004.11:g.81207599A>G , CM000666.1:g.81207599A>G GRCh37
NC_000004.10:g.81426623A>G NCBI36
NG_029501.1:g.24858A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000312465.12:c.580A>G MANE Select ENSP00000311697.7:p.Lys194Glu
ENST00000312465.11:c.580A>G ENSP00000311697.7:p.Lys194Glu
ENST00000456523.3:c.*104A>G ENSP00000398353.3:n.*104A>G
ENST00000503413.1:n.529A>G
ENST00000507780.1:c.342+11433A>G ENSP00000423903.1:n.342+11433A>G
NM_001291812.1:c.151A>G NP_001278741.1:p.Lys51Glu
NM_004464.3:c.580A>G NP_004455.2:p.Lys194Glu
NM_033143.2:c.*104A>G NP_149134.1:n.*104A>G
NM_001291812.2:c.151A>G NP_001278741.1:p.Lys51Glu
NM_004464.4:c.580A>G MANE Select NP_004455.2:p.Lys194Glu