Canonical Allele Identifier: CA377834435

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531279G>C (hg19) ; chr10:g.101771522G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771522G>C , CM000672.2:g.101771522G>C	GRCh38
NC_000010.10:g.103531279G>C , CM000672.1:g.103531279G>C	GRCh37
NC_000010.9:g.103521269G>C	NCBI36
NG_007151.1:g.9549C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.385C>G MANE Select	ENSP00000321797.2:p.Arg129Gly
ENST00000618991.5:c.73C>G	ENSP00000484420.1:p.Arg25Gly
ENST00000344255.8:c.352C>G	ENSP00000340039.3:p.Arg118Gly
ENST00000320185.6:c.385C>G	ENSP00000321797.2:p.Arg129Gly
ENST00000344255.7:c.352C>G	ENSP00000340039.3:p.Arg118Gly
ENST00000346714.7:c.265C>G	ENSP00000344306.3:p.Arg89Gly
ENST00000347978.2:c.298C>G	ENSP00000321945.2:p.Arg100Gly
ENST00000469792.6:c.*349C>G	ENSP00000473299.1:n.*349C>G
ENST00000485728.1:n.261C>G
ENST00000618991.4:c.73C>G	ENSP00000484420.1:p.Arg25Gly
NM_001206389.1:c.73C>G	NP_001193318.1:p.Arg25Gly
NM_006119.4:c.298C>G	NP_006110.1:p.Arg100Gly
NM_033163.3:c.385C>G	NP_149353.1:p.Arg129Gly
NM_033164.3:c.352C>G	NP_149354.1:p.Arg118Gly
NM_033165.3:c.265C>G	NP_149355.1:p.Arg89Gly
XM_011539509.1:c.307C>G	XP_011537811.1:p.Arg103Gly
XR_946251.1:n.303G>C
XR_946252.1:n.234G>C
XR_946253.1:n.232G>C
XR_946252.2:n.324G>C
XR_946253.2:n.322G>C
NM_006119.5:c.298C>G	NP_006110.1:p.Arg100Gly
NM_033163.4:c.385C>G	NP_149353.1:p.Arg129Gly
NM_033164.4:c.352C>G	NP_149354.1:p.Arg118Gly
NM_033165.4:c.265C>G	NP_149355.1:p.Arg89Gly
NM_001206389.2:c.73C>G	NP_001193318.1:p.Arg25Gly
NM_006119.6:c.298C>G	NP_006110.1:p.Arg100Gly
NM_033163.5:c.385C>G MANE Select	NP_149353.1:p.Arg129Gly
NM_033165.5:c.265C>G	NP_149355.1:p.Arg89Gly