Canonical Allele Identifier: CA1932376767

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774853C= , CM000672.2:g.101774853C=	GRCh38
NC_000010.10:g.103534610C= , CM000672.1:g.103534610C=	GRCh37
NC_000010.9:g.103524600C=	NCBI36
NG_007151.1:g.6218G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.216G= MANE Select	ENSP00000321797.2:p.Thr72=
ENST00000618991.5:c.-97G=	ENSP00000484420.1:n.-97G=
ENST00000344255.8:c.183G=	ENSP00000340039.3:p.Thr61=
ENST00000320185.6:c.216G=	ENSP00000321797.2:p.Thr72=
ENST00000344255.7:c.183G=	ENSP00000340039.3:p.Thr61=
ENST00000346714.7:c.96G=	ENSP00000344306.3:p.Thr32=
ENST00000347978.2:c.129G=	ENSP00000321945.2:p.Thr43=
ENST00000469792.6:c.*180G=	ENSP00000473299.1:n.*180G=
ENST00000485728.1:n.92G=
ENST00000618991.4:c.-97G=	ENSP00000484420.1:n.-97G=
NM_001206389.1:c.-97G=	NP_001193318.1:n.-97G=
NM_006119.4:c.129G=	NP_006110.1:p.Thr43=
NM_033163.3:c.216G=	NP_149353.1:p.Thr72=
NM_033164.3:c.183G=	NP_149354.1:p.Thr61=
NM_033165.3:c.96G=	NP_149355.1:p.Thr32=
XM_011539509.1:c.138G=	XP_011537811.1:p.Thr46=
NM_006119.5:c.129G=	NP_006110.1:p.Thr43=
NM_033163.4:c.216G=	NP_149353.1:p.Thr72=
NM_033164.4:c.183G=	NP_149354.1:p.Thr61=
NM_033165.4:c.96G=	NP_149355.1:p.Thr32=
NM_001206389.2:c.-97G=	NP_001193318.1:n.-97G=
NM_006119.6:c.129G=	NP_006110.1:p.Thr43=
NM_033163.5:c.216G= MANE Select	NP_149353.1:p.Thr72=
NM_033165.5:c.96G=	NP_149355.1:p.Thr32=