Canonical Allele Identifier: CA440227718

Gene: FGF5

Linked Data

• MyVariant Identifiers: chr4:g.81207529C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286375C>T , CM000666.2:g.80286375C>T	GRCh38
NC_000004.11:g.81207529C>T , CM000666.1:g.81207529C>T	GRCh37
NC_000004.10:g.81426553C>T	NCBI36
NG_029501.1:g.24788C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.510C>T MANE Select	ENSP00000311697.7:p.Ser170=
ENST00000312465.11:c.510C>T	ENSP00000311697.7:p.Ser170=
ENST00000456523.3:c.*34C>T	ENSP00000398353.3:n.*34C>T
ENST00000503413.1:n.459C>T
ENST00000507780.1:c.342+11363C>T	ENSP00000423903.1:n.342+11363C>T
NM_001291812.1:c.81C>T	NP_001278741.1:p.Ser27=
NM_004464.3:c.510C>T	NP_004455.2:p.Ser170=
NM_033143.2:c.*34C>T	NP_149134.1:n.*34C>T
NM_001291812.2:c.81C>T	NP_001278741.1:p.Ser27=
NM_004464.4:c.510C>T MANE Select	NP_004455.2:p.Ser170=