Canonical Allele Identifier: CA377836082

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534492A>C (hg19) ; chr10:g.101774735A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774735A>C , CM000672.2:g.101774735A>C	GRCh38
NC_000010.10:g.103534492A>C , CM000672.1:g.103534492A>C	GRCh37
NC_000010.9:g.103524482A>C	NCBI36
NG_007151.1:g.6336T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.334T>G MANE Select	ENSP00000321797.2:p.Phe112Val
ENST00000618991.5:c.22T>G	ENSP00000484420.1:p.Phe8Val
ENST00000344255.8:c.301T>G	ENSP00000340039.3:p.Phe101Val
ENST00000320185.6:c.334T>G	ENSP00000321797.2:p.Phe112Val
ENST00000344255.7:c.301T>G	ENSP00000340039.3:p.Phe101Val
ENST00000346714.7:c.214T>G	ENSP00000344306.3:p.Phe72Val
ENST00000347978.2:c.247T>G	ENSP00000321945.2:p.Phe83Val
ENST00000469792.6:c.*298T>G	ENSP00000473299.1:n.*298T>G
ENST00000485728.1:n.210T>G
ENST00000618991.4:c.22T>G	ENSP00000484420.1:p.Phe8Val
NM_001206389.1:c.22T>G	NP_001193318.1:p.Phe8Val
NM_006119.4:c.247T>G	NP_006110.1:p.Phe83Val
NM_033163.3:c.334T>G	NP_149353.1:p.Phe112Val
NM_033164.3:c.301T>G	NP_149354.1:p.Phe101Val
NM_033165.3:c.214T>G	NP_149355.1:p.Phe72Val
XM_011539509.1:c.256T>G	XP_011537811.1:p.Phe86Val
NM_006119.5:c.247T>G	NP_006110.1:p.Phe83Val
NM_033163.4:c.334T>G	NP_149353.1:p.Phe112Val
NM_033164.4:c.301T>G	NP_149354.1:p.Phe101Val
NM_033165.4:c.214T>G	NP_149355.1:p.Phe72Val
NM_001206389.2:c.22T>G	NP_001193318.1:p.Phe8Val
NM_006119.6:c.247T>G	NP_006110.1:p.Phe83Val
NM_033163.5:c.334T>G MANE Select	NP_149353.1:p.Phe112Val
NM_033165.5:c.214T>G	NP_149355.1:p.Phe72Val