Canonical Allele Identifier: CA470996223

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531325T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771568T>A , CM000672.2:g.101771568T>A	GRCh38
NC_000010.10:g.103531325T>A , CM000672.1:g.103531325T>A	GRCh37
NC_000010.9:g.103521315T>A	NCBI36
NG_007151.1:g.9503A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.339A>T MANE Select	ENSP00000321797.2:p.Ala113=
ENST00000618991.5:c.27A>T	ENSP00000484420.1:p.Ala9=
ENST00000344255.8:c.306A>T	ENSP00000340039.3:p.Ala102=
ENST00000320185.6:c.339A>T	ENSP00000321797.2:p.Ala113=
ENST00000344255.7:c.306A>T	ENSP00000340039.3:p.Ala102=
ENST00000346714.7:c.219A>T	ENSP00000344306.3:p.Ala73=
ENST00000347978.2:c.252A>T	ENSP00000321945.2:p.Ala84=
ENST00000469792.6:c.*303A>T	ENSP00000473299.1:n.*303A>T
ENST00000485728.1:n.215A>T
ENST00000618991.4:c.27A>T	ENSP00000484420.1:p.Ala9=
NM_001206389.1:c.27A>T	NP_001193318.1:p.Ala9=
NM_006119.4:c.252A>T	NP_006110.1:p.Ala84=
NM_033163.3:c.339A>T	NP_149353.1:p.Ala113=
NM_033164.3:c.306A>T	NP_149354.1:p.Ala102=
NM_033165.3:c.219A>T	NP_149355.1:p.Ala73=
XM_011539509.1:c.261A>T	XP_011537811.1:p.Ala87=
XR_946251.1:n.349T>A
XR_946252.1:n.280T>A
XR_946253.1:n.278T>A
XR_946252.2:n.370T>A
XR_946253.2:n.368T>A
NM_006119.5:c.252A>T	NP_006110.1:p.Ala84=
NM_033163.4:c.339A>T	NP_149353.1:p.Ala113=
NM_033164.4:c.306A>T	NP_149354.1:p.Ala102=
NM_033165.4:c.219A>T	NP_149355.1:p.Ala73=
NM_001206389.2:c.27A>T	NP_001193318.1:p.Ala9=
NM_006119.6:c.252A>T	NP_006110.1:p.Ala84=
NM_033163.5:c.339A>T MANE Select	NP_149353.1:p.Ala113=
NM_033165.5:c.219A>T	NP_149355.1:p.Ala73=