Canonical Allele Identifier: CA377834475

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531291T>C (hg19) ; chr10:g.101771534T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771534T>C , CM000672.2:g.101771534T>C	GRCh38
NC_000010.10:g.103531291T>C , CM000672.1:g.103531291T>C	GRCh37
NC_000010.9:g.103521281T>C	NCBI36
NG_007151.1:g.9537A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.373A>G MANE Select	ENSP00000321797.2:p.Arg125Gly
ENST00000618991.5:c.61A>G	ENSP00000484420.1:p.Arg21Gly
ENST00000344255.8:c.340A>G	ENSP00000340039.3:p.Arg114Gly
ENST00000320185.6:c.373A>G	ENSP00000321797.2:p.Arg125Gly
ENST00000344255.7:c.340A>G	ENSP00000340039.3:p.Arg114Gly
ENST00000346714.7:c.253A>G	ENSP00000344306.3:p.Arg85Gly
ENST00000347978.2:c.286A>G	ENSP00000321945.2:p.Arg96Gly
ENST00000469792.6:c.*337A>G	ENSP00000473299.1:n.*337A>G
ENST00000485728.1:n.249A>G
ENST00000618991.4:c.61A>G	ENSP00000484420.1:p.Arg21Gly
NM_001206389.1:c.61A>G	NP_001193318.1:p.Arg21Gly
NM_006119.4:c.286A>G	NP_006110.1:p.Arg96Gly
NM_033163.3:c.373A>G	NP_149353.1:p.Arg125Gly
NM_033164.3:c.340A>G	NP_149354.1:p.Arg114Gly
NM_033165.3:c.253A>G	NP_149355.1:p.Arg85Gly
XM_011539509.1:c.295A>G	XP_011537811.1:p.Arg99Gly
XR_946251.1:n.315T>C
XR_946252.1:n.246T>C
XR_946253.1:n.244T>C
XR_946252.2:n.336T>C
XR_946253.2:n.334T>C
NM_006119.5:c.286A>G	NP_006110.1:p.Arg96Gly
NM_033163.4:c.373A>G	NP_149353.1:p.Arg125Gly
NM_033164.4:c.340A>G	NP_149354.1:p.Arg114Gly
NM_033165.4:c.253A>G	NP_149355.1:p.Arg85Gly
NM_001206389.2:c.61A>G	NP_001193318.1:p.Arg21Gly
NM_006119.6:c.286A>G	NP_006110.1:p.Arg96Gly
NM_033163.5:c.373A>G MANE Select	NP_149353.1:p.Arg125Gly
NM_033165.5:c.253A>G	NP_149355.1:p.Arg85Gly