Canonical Allele Identifier: CA2982757

Gene: FGF5

Linked Data

• dbSNP Id: rs368904140
• ExAC: 4:81207806 C / T
• gnomAD v2: 4-81207806-C-T
• gnomAD v3: 4-80286652-C-T
• gnomAD v4: 4-80286652-C-T
• MyVariant Identifiers: chr4:g.81207806C>T (hg19) ; chr4:g.80286652C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286652C>T , CM000666.2:g.80286652C>T	GRCh38
NC_000004.11:g.81207806C>T , CM000666.1:g.81207806C>T	GRCh37
NC_000004.10:g.81426830C>T	NCBI36
NG_029501.1:g.25065C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.787C>T MANE Select	ENSP00000311697.7:p.Leu263Phe
ENST00000312465.11:c.787C>T	ENSP00000311697.7:p.Leu263Phe
ENST00000456523.3:c.*311C>T	ENSP00000398353.3:n.*311C>T
ENST00000503413.1:n.736C>T
ENST00000507780.1:c.342+11640C>T	ENSP00000423903.1:n.342+11640C>T
NM_001291812.1:c.358C>T	NP_001278741.1:p.Leu120Phe
NM_004464.3:c.787C>T	NP_004455.2:p.Leu263Phe
NM_033143.2:c.*311C>T	NP_149134.1:n.*311C>T
NM_001291812.2:c.358C>T	NP_001278741.1:p.Leu120Phe
NM_004464.4:c.787C>T MANE Select	NP_004455.2:p.Leu263Phe