Canonical Allele Identifier: CA440227752

Gene: FGF5

Linked Data

• MyVariant Identifiers: chr4:g.81207826A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286672A>G , CM000666.2:g.80286672A>G	GRCh38
NC_000004.11:g.81207826A>G , CM000666.1:g.81207826A>G	GRCh37
NC_000004.10:g.81426850A>G	NCBI36
NG_029501.1:g.25085A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.807A>G MANE Select	ENSP00000311697.7:p.Ter269=
ENST00000312465.11:c.807A>G	ENSP00000311697.7:p.Ter269=
ENST00000456523.3:c.*331A>G	ENSP00000398353.3:n.*331A>G
ENST00000503413.1:n.756A>G
ENST00000507780.1:c.342+11660A>G	ENSP00000423903.1:n.342+11660A>G
NM_001291812.1:c.378A>G	NP_001278741.1:p.Ter126=
NM_004464.3:c.807A>G	NP_004455.2:p.Ter269=
NM_033143.2:c.*331A>G	NP_149134.1:n.*331A>G
NM_001291812.2:c.378A>G	NP_001278741.1:p.Ter126=
NM_004464.4:c.807A>G MANE Select	NP_004455.2:p.Ter269=