Canonical Allele Identifier: CA377834929

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531321G>C (hg19) ; chr10:g.101771564G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771564G>C , CM000672.2:g.101771564G>C	GRCh38
NC_000010.10:g.103531321G>C , CM000672.1:g.103531321G>C	GRCh37
NC_000010.9:g.103521311G>C	NCBI36
NG_007151.1:g.9507C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.343C>G MANE Select	ENSP00000321797.2:p.Leu115Val
ENST00000618991.5:c.31C>G	ENSP00000484420.1:p.Leu11Val
ENST00000344255.8:c.310C>G	ENSP00000340039.3:p.Leu104Val
ENST00000320185.6:c.343C>G	ENSP00000321797.2:p.Leu115Val
ENST00000344255.7:c.310C>G	ENSP00000340039.3:p.Leu104Val
ENST00000346714.7:c.223C>G	ENSP00000344306.3:p.Leu75Val
ENST00000347978.2:c.256C>G	ENSP00000321945.2:p.Leu86Val
ENST00000469792.6:c.*307C>G	ENSP00000473299.1:n.*307C>G
ENST00000485728.1:n.219C>G
ENST00000618991.4:c.31C>G	ENSP00000484420.1:p.Leu11Val
NM_001206389.1:c.31C>G	NP_001193318.1:p.Leu11Val
NM_006119.4:c.256C>G	NP_006110.1:p.Leu86Val
NM_033163.3:c.343C>G	NP_149353.1:p.Leu115Val
NM_033164.3:c.310C>G	NP_149354.1:p.Leu104Val
NM_033165.3:c.223C>G	NP_149355.1:p.Leu75Val
XM_011539509.1:c.265C>G	XP_011537811.1:p.Leu89Val
XR_946251.1:n.345G>C
XR_946252.1:n.276G>C
XR_946253.1:n.274G>C
XR_946252.2:n.366G>C
XR_946253.2:n.364G>C
NM_006119.5:c.256C>G	NP_006110.1:p.Leu86Val
NM_033163.4:c.343C>G	NP_149353.1:p.Leu115Val
NM_033164.4:c.310C>G	NP_149354.1:p.Leu104Val
NM_033165.4:c.223C>G	NP_149355.1:p.Leu75Val
NM_001206389.2:c.31C>G	NP_001193318.1:p.Leu11Val
NM_006119.6:c.256C>G	NP_006110.1:p.Leu86Val
NM_033163.5:c.343C>G MANE Select	NP_149353.1:p.Leu115Val
NM_033165.5:c.223C>G	NP_149355.1:p.Leu75Val