Canonical Allele Identifier: CA1471368403

Gene: FGF5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286415A= , CM000666.2:g.80286415A=	GRCh38
NC_000004.11:g.81207569A= , CM000666.1:g.81207569A=	GRCh37
NC_000004.10:g.81426593A=	NCBI36
NG_029501.1:g.24828A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.550A= MANE Select	ENSP00000311697.7:p.Thr184=
ENST00000312465.11:c.550A=	ENSP00000311697.7:p.Thr184=
ENST00000456523.3:c.*74A=	ENSP00000398353.3:n.*74A=
ENST00000503413.1:n.499A=
ENST00000507780.1:c.342+11403A=	ENSP00000423903.1:n.342+11403A=
NM_001291812.1:c.121A=	NP_001278741.1:p.Thr41=
NM_004464.3:c.550A=	NP_004455.2:p.Thr184=
NM_033143.2:c.*74A=	NP_149134.1:n.*74A=
NM_001291812.2:c.121A=	NP_001278741.1:p.Thr41=
NM_004464.4:c.550A= MANE Select	NP_004455.2:p.Thr184=