Canonical Allele Identifier: CA357396923

Gene: FGF5

Linked Data

• MyVariant Identifiers: chr4:g.81207521G>A (hg19) ; chr4:g.80286367G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286367G>A , CM000666.2:g.80286367G>A	GRCh38
NC_000004.11:g.81207521G>A , CM000666.1:g.81207521G>A	GRCh37
NC_000004.10:g.81426545G>A	NCBI36
NG_029501.1:g.24780G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.502G>A MANE Select	ENSP00000311697.7:p.Glu168Lys
ENST00000312465.11:c.502G>A	ENSP00000311697.7:p.Glu168Lys
ENST00000456523.3:c.*26G>A	ENSP00000398353.3:n.*26G>A
ENST00000503413.1:n.451G>A
ENST00000507780.1:c.342+11355G>A	ENSP00000423903.1:n.342+11355G>A
NM_001291812.1:c.73G>A	NP_001278741.1:p.Glu25Lys
NM_004464.3:c.502G>A	NP_004455.2:p.Glu168Lys
NM_033143.2:c.*26G>A	NP_149134.1:n.*26G>A
NM_001291812.2:c.73G>A	NP_001278741.1:p.Glu25Lys
NM_004464.4:c.502G>A MANE Select	NP_004455.2:p.Glu168Lys