Canonical Allele Identifier: CA357397201
Gene: FGF5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.81207546C>A (hg19) chr4:g.80286392C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80286392C>A , CM000666.2:g.80286392C>A GRCh38
NC_000004.11:g.81207546C>A , CM000666.1:g.81207546C>A GRCh37
NC_000004.10:g.81426570C>A NCBI36
NG_029501.1:g.24805C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000312465.12:c.527C>A MANE Select ENSP00000311697.7:p.Ser176Ter
ENST00000312465.11:c.527C>A ENSP00000311697.7:p.Ser176Ter
ENST00000456523.3:c.*51C>A ENSP00000398353.3:n.*51C>A
ENST00000503413.1:n.476C>A
ENST00000507780.1:c.342+11380C>A ENSP00000423903.1:n.342+11380C>A
NM_001291812.1:c.98C>A NP_001278741.1:p.Ser33Ter
NM_004464.3:c.527C>A NP_004455.2:p.Ser176Ter
NM_033143.2:c.*51C>A NP_149134.1:n.*51C>A
NM_001291812.2:c.98C>A NP_001278741.1:p.Ser33Ter
NM_004464.4:c.527C>A MANE Select NP_004455.2:p.Ser176Ter
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