Canonical Allele Identifier: CA2982741
Gene: FGF5 HGNC NCBI

Linked Data

dbSNP Id: rs141185778
gnomAD v2: 4-81207737-C-T
gnomAD v3: 4-80286583-C-T
gnomAD v4: 4-80286583-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80286583C>T , CM000666.2:g.80286583C>T GRCh38
NC_000004.11:g.81207737C>T , CM000666.1:g.81207737C>T GRCh37
NC_000004.10:g.81426761C>T NCBI36
NG_029501.1:g.24996C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000312465.12:c.718C>T MANE Select ENSP00000311697.7:p.Pro240Ser
ENST00000312465.11:c.718C>T ENSP00000311697.7:p.Pro240Ser
ENST00000456523.3:c.*242C>T ENSP00000398353.3:n.*242C>T
ENST00000503413.1:n.667C>T
ENST00000507780.1:c.342+11571C>T ENSP00000423903.1:n.342+11571C>T
NM_001291812.1:c.289C>T NP_001278741.1:p.Pro97Ser
NM_004464.3:c.718C>T NP_004455.2:p.Pro240Ser
NM_033143.2:c.*242C>T NP_149134.1:n.*242C>T
NM_001291812.2:c.289C>T NP_001278741.1:p.Pro97Ser
NM_004464.4:c.718C>T MANE Select NP_004455.2:p.Pro240Ser