Canonical Allele Identifier: CA357399198

Gene: FGF5

Linked Data

• gnomAD v4: 4-80286632-C-G
• MyVariant Identifiers: chr4:g.81207786C>G (hg19) ; chr4:g.80286632C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286632C>G , CM000666.2:g.80286632C>G	GRCh38
NC_000004.11:g.81207786C>G , CM000666.1:g.81207786C>G	GRCh37
NC_000004.10:g.81426810C>G	NCBI36
NG_029501.1:g.25045C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.767C>G MANE Select	ENSP00000311697.7:p.Thr256Ser
ENST00000312465.11:c.767C>G	ENSP00000311697.7:p.Thr256Ser
ENST00000456523.3:c.*291C>G	ENSP00000398353.3:n.*291C>G
ENST00000503413.1:n.716C>G
ENST00000507780.1:c.342+11620C>G	ENSP00000423903.1:n.342+11620C>G
NM_001291812.1:c.338C>G	NP_001278741.1:p.Thr113Ser
NM_004464.3:c.767C>G	NP_004455.2:p.Thr256Ser
NM_033143.2:c.*291C>G	NP_149134.1:n.*291C>G
NM_001291812.2:c.338C>G	NP_001278741.1:p.Thr113Ser
NM_004464.4:c.767C>G MANE Select	NP_004455.2:p.Thr256Ser