Canonical Allele Identifier: CA357399056

Gene: FGF5

Linked Data

• MyVariant Identifiers: chr4:g.81207770G>C (hg19) ; chr4:g.80286616G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286616G>C , CM000666.2:g.80286616G>C	GRCh38
NC_000004.11:g.81207770G>C , CM000666.1:g.81207770G>C	GRCh37
NC_000004.10:g.81426794G>C	NCBI36
NG_029501.1:g.25029G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.751G>C MANE Select	ENSP00000311697.7:p.Ala251Pro
ENST00000312465.11:c.751G>C	ENSP00000311697.7:p.Ala251Pro
ENST00000456523.3:c.*275G>C	ENSP00000398353.3:n.*275G>C
ENST00000503413.1:n.700G>C
ENST00000507780.1:c.342+11604G>C	ENSP00000423903.1:n.342+11604G>C
NM_001291812.1:c.322G>C	NP_001278741.1:p.Ala108Pro
NM_004464.3:c.751G>C	NP_004455.2:p.Ala251Pro
NM_033143.2:c.*275G>C	NP_149134.1:n.*275G>C
NM_001291812.2:c.322G>C	NP_001278741.1:p.Ala108Pro
NM_004464.4:c.751G>C MANE Select	NP_004455.2:p.Ala251Pro