Canonical Allele Identifier: CA470996046

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531271G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771514G>C , CM000672.2:g.101771514G>C	GRCh38
NC_000010.10:g.103531271G>C , CM000672.1:g.103531271G>C	GRCh37
NC_000010.9:g.103521261G>C	NCBI36
NG_007151.1:g.9557C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.393C>G MANE Select	ENSP00000321797.2:p.Ala131=
ENST00000618991.5:c.81C>G	ENSP00000484420.1:p.Ala27=
ENST00000344255.8:c.360C>G	ENSP00000340039.3:p.Ala120=
ENST00000320185.6:c.393C>G	ENSP00000321797.2:p.Ala131=
ENST00000344255.7:c.360C>G	ENSP00000340039.3:p.Ala120=
ENST00000346714.7:c.273C>G	ENSP00000344306.3:p.Ala91=
ENST00000347978.2:c.306C>G	ENSP00000321945.2:p.Ala102=
ENST00000469792.6:c.*357C>G	ENSP00000473299.1:n.*357C>G
ENST00000485728.1:n.269C>G
ENST00000618991.4:c.81C>G	ENSP00000484420.1:p.Ala27=
NM_001206389.1:c.81C>G	NP_001193318.1:p.Ala27=
NM_006119.4:c.306C>G	NP_006110.1:p.Ala102=
NM_033163.3:c.393C>G	NP_149353.1:p.Ala131=
NM_033164.3:c.360C>G	NP_149354.1:p.Ala120=
NM_033165.3:c.273C>G	NP_149355.1:p.Ala91=
XM_011539509.1:c.315C>G	XP_011537811.1:p.Ala105=
XR_946251.1:n.295G>C
XR_946252.1:n.226G>C
XR_946253.1:n.224G>C
XR_946252.2:n.316G>C
XR_946253.2:n.314G>C
NM_006119.5:c.306C>G	NP_006110.1:p.Ala102=
NM_033163.4:c.393C>G	NP_149353.1:p.Ala131=
NM_033164.4:c.360C>G	NP_149354.1:p.Ala120=
NM_033165.4:c.273C>G	NP_149355.1:p.Ala91=
NM_001206389.2:c.81C>G	NP_001193318.1:p.Ala27=
NM_006119.6:c.306C>G	NP_006110.1:p.Ala102=
NM_033163.5:c.393C>G MANE Select	NP_149353.1:p.Ala131=
NM_033165.5:c.273C>G	NP_149355.1:p.Ala91=