Canonical Allele Identifier: CA377834862

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531309T>C (hg19) ; chr10:g.101771552T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771552T>C , CM000672.2:g.101771552T>C	GRCh38
NC_000010.10:g.103531309T>C , CM000672.1:g.103531309T>C	GRCh37
NC_000010.9:g.103521299T>C	NCBI36
NG_007151.1:g.9519A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.355A>G MANE Select	ENSP00000321797.2:p.Thr119Ala
ENST00000618991.5:c.43A>G	ENSP00000484420.1:p.Thr15Ala
ENST00000344255.8:c.322A>G	ENSP00000340039.3:p.Thr108Ala
ENST00000320185.6:c.355A>G	ENSP00000321797.2:p.Thr119Ala
ENST00000344255.7:c.322A>G	ENSP00000340039.3:p.Thr108Ala
ENST00000346714.7:c.235A>G	ENSP00000344306.3:p.Thr79Ala
ENST00000347978.2:c.268A>G	ENSP00000321945.2:p.Thr90Ala
ENST00000469792.6:c.*319A>G	ENSP00000473299.1:n.*319A>G
ENST00000485728.1:n.231A>G
ENST00000618991.4:c.43A>G	ENSP00000484420.1:p.Thr15Ala
NM_001206389.1:c.43A>G	NP_001193318.1:p.Thr15Ala
NM_006119.4:c.268A>G	NP_006110.1:p.Thr90Ala
NM_033163.3:c.355A>G	NP_149353.1:p.Thr119Ala
NM_033164.3:c.322A>G	NP_149354.1:p.Thr108Ala
NM_033165.3:c.235A>G	NP_149355.1:p.Thr79Ala
XM_011539509.1:c.277A>G	XP_011537811.1:p.Thr93Ala
XR_946251.1:n.333T>C
XR_946252.1:n.264T>C
XR_946253.1:n.262T>C
XR_946252.2:n.354T>C
XR_946253.2:n.352T>C
NM_006119.5:c.268A>G	NP_006110.1:p.Thr90Ala
NM_033163.4:c.355A>G	NP_149353.1:p.Thr119Ala
NM_033164.4:c.322A>G	NP_149354.1:p.Thr108Ala
NM_033165.4:c.235A>G	NP_149355.1:p.Thr79Ala
NM_001206389.2:c.43A>G	NP_001193318.1:p.Thr15Ala
NM_006119.6:c.268A>G	NP_006110.1:p.Thr90Ala
NM_033163.5:c.355A>G MANE Select	NP_149353.1:p.Thr119Ala
NM_033165.5:c.235A>G	NP_149355.1:p.Thr79Ala