Canonical Allele Identifier: CA470996075

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531286A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771529A>C , CM000672.2:g.101771529A>C	GRCh38
NC_000010.10:g.103531286A>C , CM000672.1:g.103531286A>C	GRCh37
NC_000010.9:g.103521276A>C	NCBI36
NG_007151.1:g.9542T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000320185.7:c.378T>G MANE Select	ENSP00000321797.2:p.Val126=
ENST00000618991.5:c.66T>G	ENSP00000484420.1:p.Val22=
ENST00000344255.8:c.345T>G	ENSP00000340039.3:p.Val115=
ENST00000320185.6:c.378T>G	ENSP00000321797.2:p.Val126=
ENST00000344255.7:c.345T>G	ENSP00000340039.3:p.Val115=
ENST00000346714.7:c.258T>G	ENSP00000344306.3:p.Val86=
ENST00000347978.2:c.291T>G	ENSP00000321945.2:p.Val97=
ENST00000469792.6:c.*342T>G	ENSP00000473299.1:n.*342T>G
ENST00000485728.1:n.254T>G
ENST00000618991.4:c.66T>G	ENSP00000484420.1:p.Val22=
NM_001206389.1:c.66T>G	NP_001193318.1:p.Val22=
NM_006119.4:c.291T>G	NP_006110.1:p.Val97=
NM_033163.3:c.378T>G	NP_149353.1:p.Val126=
NM_033164.3:c.345T>G	NP_149354.1:p.Val115=
NM_033165.3:c.258T>G	NP_149355.1:p.Val86=
XM_011539509.1:c.300T>G	XP_011537811.1:p.Val100=
XR_946251.1:n.310A>C
XR_946252.1:n.241A>C
XR_946253.1:n.239A>C
XR_946252.2:n.331A>C
XR_946253.2:n.329A>C
NM_006119.5:c.291T>G	NP_006110.1:p.Val97=
NM_033163.4:c.378T>G	NP_149353.1:p.Val126=
NM_033164.4:c.345T>G	NP_149354.1:p.Val115=
NM_033165.4:c.258T>G	NP_149355.1:p.Val86=
NM_001206389.2:c.66T>G	NP_001193318.1:p.Val22=
NM_006119.6:c.291T>G	NP_006110.1:p.Val97=
NM_033163.5:c.378T>G MANE Select	NP_149353.1:p.Val126=
NM_033165.5:c.258T>G	NP_149355.1:p.Val86=