Canonical Allele Identifier: CA357397788
Gene: FGF5 HGNC NCBI

Linked Data

dbSNP Id: rs1308454307
gnomAD v2: 4-81207623-T-G
gnomAD v3: 4-80286469-T-G
gnomAD v4: 4-80286469-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80286469T>G , CM000666.2:g.80286469T>G GRCh38
NC_000004.11:g.81207623T>G , CM000666.1:g.81207623T>G GRCh37
NC_000004.10:g.81426647T>G NCBI36
NG_029501.1:g.24882T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000312465.12:c.604T>G MANE Select ENSP00000311697.7:p.Cys202Gly
ENST00000312465.11:c.604T>G ENSP00000311697.7:p.Cys202Gly
ENST00000456523.3:c.*128T>G ENSP00000398353.3:n.*128T>G
ENST00000503413.1:n.553T>G
ENST00000507780.1:c.342+11457T>G ENSP00000423903.1:n.342+11457T>G
NM_001291812.1:c.175T>G NP_001278741.1:p.Cys59Gly
NM_004464.3:c.604T>G NP_004455.2:p.Cys202Gly
NM_033143.2:c.*128T>G NP_149134.1:n.*128T>G
NM_001291812.2:c.175T>G NP_001278741.1:p.Cys59Gly
NM_004464.4:c.604T>G MANE Select NP_004455.2:p.Cys202Gly