Canonical Allele Identifier: CA357397189
Gene: FGF5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.81207545T>A (hg19) chr4:g.80286391T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80286391T>A , CM000666.2:g.80286391T>A GRCh38
NC_000004.11:g.81207545T>A , CM000666.1:g.81207545T>A GRCh37
NC_000004.10:g.81426569T>A NCBI36
NG_029501.1:g.24804T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000312465.12:c.526T>A MANE Select ENSP00000311697.7:p.Ser176Thr
ENST00000312465.11:c.526T>A ENSP00000311697.7:p.Ser176Thr
ENST00000456523.3:c.*50T>A ENSP00000398353.3:n.*50T>A
ENST00000503413.1:n.475T>A
ENST00000507780.1:c.342+11379T>A ENSP00000423903.1:n.342+11379T>A
NM_001291812.1:c.97T>A NP_001278741.1:p.Ser33Thr
NM_004464.3:c.526T>A NP_004455.2:p.Ser176Thr
NM_033143.2:c.*50T>A NP_149134.1:n.*50T>A
NM_001291812.2:c.97T>A NP_001278741.1:p.Ser33Thr
NM_004464.4:c.526T>A MANE Select NP_004455.2:p.Ser176Thr
Search 100 bp 5'
Search 100 bp 3'