Canonical Allele Identifier: CA377834498

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531299A>C (hg19) ; chr10:g.101771542A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771542A>C , CM000672.2:g.101771542A>C	GRCh38
NC_000010.10:g.103531299A>C , CM000672.1:g.103531299A>C	GRCh37
NC_000010.9:g.103521289A>C	NCBI36
NG_007151.1:g.9529T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.365T>G MANE Select	ENSP00000321797.2:p.Phe122Cys
ENST00000618991.5:c.53T>G	ENSP00000484420.1:p.Phe18Cys
ENST00000344255.8:c.332T>G	ENSP00000340039.3:p.Phe111Cys
ENST00000320185.6:c.365T>G	ENSP00000321797.2:p.Phe122Cys
ENST00000344255.7:c.332T>G	ENSP00000340039.3:p.Phe111Cys
ENST00000346714.7:c.245T>G	ENSP00000344306.3:p.Phe82Cys
ENST00000347978.2:c.278T>G	ENSP00000321945.2:p.Phe93Cys
ENST00000469792.6:c.*329T>G	ENSP00000473299.1:n.*329T>G
ENST00000485728.1:n.241T>G
ENST00000618991.4:c.53T>G	ENSP00000484420.1:p.Phe18Cys
NM_001206389.1:c.53T>G	NP_001193318.1:p.Phe18Cys
NM_006119.4:c.278T>G	NP_006110.1:p.Phe93Cys
NM_033163.3:c.365T>G	NP_149353.1:p.Phe122Cys
NM_033164.3:c.332T>G	NP_149354.1:p.Phe111Cys
NM_033165.3:c.245T>G	NP_149355.1:p.Phe82Cys
XM_011539509.1:c.287T>G	XP_011537811.1:p.Phe96Cys
XR_946251.1:n.323A>C
XR_946252.1:n.254A>C
XR_946253.1:n.252A>C
XR_946252.2:n.344A>C
XR_946253.2:n.342A>C
NM_006119.5:c.278T>G	NP_006110.1:p.Phe93Cys
NM_033163.4:c.365T>G	NP_149353.1:p.Phe122Cys
NM_033164.4:c.332T>G	NP_149354.1:p.Phe111Cys
NM_033165.4:c.245T>G	NP_149355.1:p.Phe82Cys
NM_001206389.2:c.53T>G	NP_001193318.1:p.Phe18Cys
NM_006119.6:c.278T>G	NP_006110.1:p.Phe93Cys
NM_033163.5:c.365T>G MANE Select	NP_149353.1:p.Phe122Cys
NM_033165.5:c.245T>G	NP_149355.1:p.Phe82Cys