Canonical Allele Identifier: CA357396966

Gene: FGF5

Linked Data

• dbSNP Id: rs1720718266
• MyVariant Identifiers: chr4:g.81207524A>C (hg19) ; chr4:g.80286370A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286370A>C , CM000666.2:g.80286370A>C	GRCh38
NC_000004.11:g.81207524A>C , CM000666.1:g.81207524A>C	GRCh37
NC_000004.10:g.81426548A>C	NCBI36
NG_029501.1:g.24783A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.505A>C MANE Select	ENSP00000311697.7:p.Asn169His
ENST00000312465.11:c.505A>C	ENSP00000311697.7:p.Asn169His
ENST00000456523.3:c.*29A>C	ENSP00000398353.3:n.*29A>C
ENST00000503413.1:n.454A>C
ENST00000507780.1:c.342+11358A>C	ENSP00000423903.1:n.342+11358A>C
NM_001291812.1:c.76A>C	NP_001278741.1:p.Asn26His
NM_004464.3:c.505A>C	NP_004455.2:p.Asn169His
NM_033143.2:c.*29A>C	NP_149134.1:n.*29A>C
NM_001291812.2:c.76A>C	NP_001278741.1:p.Asn26His
NM_004464.4:c.505A>C MANE Select	NP_004455.2:p.Asn169His