Canonical Allele Identifier: CA1932372665

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771561T= , CM000672.2:g.101771561T=	GRCh38
NC_000010.10:g.103531318T= , CM000672.1:g.103531318T=	GRCh37
NC_000010.9:g.103521308T=	NCBI36
NG_007151.1:g.9510A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.346A= MANE Select	ENSP00000321797.2:p.Ile116=
ENST00000618991.5:c.34A=	ENSP00000484420.1:p.Ile12=
ENST00000344255.8:c.313A=	ENSP00000340039.3:p.Ile105=
ENST00000320185.6:c.346A=	ENSP00000321797.2:p.Ile116=
ENST00000344255.7:c.313A=	ENSP00000340039.3:p.Ile105=
ENST00000346714.7:c.226A=	ENSP00000344306.3:p.Ile76=
ENST00000347978.2:c.259A=	ENSP00000321945.2:p.Ile87=
ENST00000469792.6:c.*310A=	ENSP00000473299.1:n.*310A=
ENST00000485728.1:n.222A=
ENST00000618991.4:c.34A=	ENSP00000484420.1:p.Ile12=
NM_001206389.1:c.34A=	NP_001193318.1:p.Ile12=
NM_006119.4:c.259A=	NP_006110.1:p.Ile87=
NM_033163.3:c.346A=	NP_149353.1:p.Ile116=
NM_033164.3:c.313A=	NP_149354.1:p.Ile105=
NM_033165.3:c.226A=	NP_149355.1:p.Ile76=
XM_011539509.1:c.268A=	XP_011537811.1:p.Ile90=
XR_946251.1:n.342T=
XR_946252.1:n.273T=
XR_946253.1:n.271T=
XR_946252.2:n.363T=
XR_946253.2:n.361T=
NM_006119.5:c.259A=	NP_006110.1:p.Ile87=
NM_033163.4:c.346A=	NP_149353.1:p.Ile116=
NM_033164.4:c.313A=	NP_149354.1:p.Ile105=
NM_033165.4:c.226A=	NP_149355.1:p.Ile76=
NM_001206389.2:c.34A=	NP_001193318.1:p.Ile12=
NM_006119.6:c.259A=	NP_006110.1:p.Ile87=
NM_033163.5:c.346A= MANE Select	NP_149353.1:p.Ile116=
NM_033165.5:c.226A=	NP_149355.1:p.Ile76=