Canonical Allele Identifier: CA377834412

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531272G>T (hg19) ; chr10:g.101771515G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771515G>T , CM000672.2:g.101771515G>T	GRCh38
NC_000010.10:g.103531272G>T , CM000672.1:g.103531272G>T	GRCh37
NC_000010.9:g.103521262G>T	NCBI36
NG_007151.1:g.9556C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.392C>A MANE Select	ENSP00000321797.2:p.Ala131Asp
ENST00000618991.5:c.80C>A	ENSP00000484420.1:p.Ala27Asp
ENST00000344255.8:c.359C>A	ENSP00000340039.3:p.Ala120Asp
ENST00000320185.6:c.392C>A	ENSP00000321797.2:p.Ala131Asp
ENST00000344255.7:c.359C>A	ENSP00000340039.3:p.Ala120Asp
ENST00000346714.7:c.272C>A	ENSP00000344306.3:p.Ala91Asp
ENST00000347978.2:c.305C>A	ENSP00000321945.2:p.Ala102Asp
ENST00000469792.6:c.*356C>A	ENSP00000473299.1:n.*356C>A
ENST00000485728.1:n.268C>A
ENST00000618991.4:c.80C>A	ENSP00000484420.1:p.Ala27Asp
NM_001206389.1:c.80C>A	NP_001193318.1:p.Ala27Asp
NM_006119.4:c.305C>A	NP_006110.1:p.Ala102Asp
NM_033163.3:c.392C>A	NP_149353.1:p.Ala131Asp
NM_033164.3:c.359C>A	NP_149354.1:p.Ala120Asp
NM_033165.3:c.272C>A	NP_149355.1:p.Ala91Asp
XM_011539509.1:c.314C>A	XP_011537811.1:p.Ala105Asp
XR_946251.1:n.296G>T
XR_946252.1:n.227G>T
XR_946253.1:n.225G>T
XR_946252.2:n.317G>T
XR_946253.2:n.315G>T
NM_006119.5:c.305C>A	NP_006110.1:p.Ala102Asp
NM_033163.4:c.392C>A	NP_149353.1:p.Ala131Asp
NM_033164.4:c.359C>A	NP_149354.1:p.Ala120Asp
NM_033165.4:c.272C>A	NP_149355.1:p.Ala91Asp
NM_001206389.2:c.80C>A	NP_001193318.1:p.Ala27Asp
NM_006119.6:c.305C>A	NP_006110.1:p.Ala102Asp
NM_033163.5:c.392C>A MANE Select	NP_149353.1:p.Ala131Asp
NM_033165.5:c.272C>A	NP_149355.1:p.Ala91Asp