Canonical Allele Identifier: CA470996100

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531295T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771538T>A , CM000672.2:g.101771538T>A	GRCh38
NC_000010.10:g.103531295T>A , CM000672.1:g.103531295T>A	GRCh37
NC_000010.9:g.103521285T>A	NCBI36
NG_007151.1:g.9533A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.369A>T MANE Select	ENSP00000321797.2:p.Gly123=
ENST00000618991.5:c.57A>T	ENSP00000484420.1:p.Gly19=
ENST00000344255.8:c.336A>T	ENSP00000340039.3:p.Gly112=
ENST00000320185.6:c.369A>T	ENSP00000321797.2:p.Gly123=
ENST00000344255.7:c.336A>T	ENSP00000340039.3:p.Gly112=
ENST00000346714.7:c.249A>T	ENSP00000344306.3:p.Gly83=
ENST00000347978.2:c.282A>T	ENSP00000321945.2:p.Gly94=
ENST00000469792.6:c.*333A>T	ENSP00000473299.1:n.*333A>T
ENST00000485728.1:n.245A>T
ENST00000618991.4:c.57A>T	ENSP00000484420.1:p.Gly19=
NM_001206389.1:c.57A>T	NP_001193318.1:p.Gly19=
NM_006119.4:c.282A>T	NP_006110.1:p.Gly94=
NM_033163.3:c.369A>T	NP_149353.1:p.Gly123=
NM_033164.3:c.336A>T	NP_149354.1:p.Gly112=
NM_033165.3:c.249A>T	NP_149355.1:p.Gly83=
XM_011539509.1:c.291A>T	XP_011537811.1:p.Gly97=
XR_946251.1:n.319T>A
XR_946252.1:n.250T>A
XR_946253.1:n.248T>A
XR_946252.2:n.340T>A
XR_946253.2:n.338T>A
NM_006119.5:c.282A>T	NP_006110.1:p.Gly94=
NM_033163.4:c.369A>T	NP_149353.1:p.Gly123=
NM_033164.4:c.336A>T	NP_149354.1:p.Gly112=
NM_033165.4:c.249A>T	NP_149355.1:p.Gly83=
NM_001206389.2:c.57A>T	NP_001193318.1:p.Gly19=
NM_006119.6:c.282A>T	NP_006110.1:p.Gly94=
NM_033163.5:c.369A>T MANE Select	NP_149353.1:p.Gly123=
NM_033165.5:c.249A>T	NP_149355.1:p.Gly83=