Canonical Allele Identifier: CA1932372501

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771500T= , CM000672.2:g.101771500T=	GRCh38
NC_000010.10:g.103531257T= , CM000672.1:g.103531257T=	GRCh37
NC_000010.9:g.103521247T=	NCBI36
NG_007151.1:g.9571A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.407A= MANE Select	ENSP00000321797.2:p.Tyr136=
ENST00000618991.5:c.95A=	ENSP00000484420.1:p.Tyr32=
ENST00000344255.8:c.374A=	ENSP00000340039.3:p.Tyr125=
ENST00000320185.6:c.407A=	ENSP00000321797.2:p.Tyr136=
ENST00000344255.7:c.374A=	ENSP00000340039.3:p.Tyr125=
ENST00000346714.7:c.287A=	ENSP00000344306.3:p.Tyr96=
ENST00000347978.2:c.320A=	ENSP00000321945.2:p.Tyr107=
ENST00000469792.6:c.*371A=	ENSP00000473299.1:n.*371A=
ENST00000485728.1:n.283A=
ENST00000618991.4:c.95A=	ENSP00000484420.1:p.Tyr32=
NM_001206389.1:c.95A=	NP_001193318.1:p.Tyr32=
NM_006119.4:c.320A=	NP_006110.1:p.Tyr107=
NM_033163.3:c.407A=	NP_149353.1:p.Tyr136=
NM_033164.3:c.374A=	NP_149354.1:p.Tyr125=
NM_033165.3:c.287A=	NP_149355.1:p.Tyr96=
XM_011539509.1:c.329A=	XP_011537811.1:p.Tyr110=
XR_946251.1:n.281T=
XR_946252.1:n.212T=
XR_946253.1:n.210T=
XR_946252.2:n.302T=
XR_946253.2:n.300T=
NM_006119.5:c.320A=	NP_006110.1:p.Tyr107=
NM_033163.4:c.407A=	NP_149353.1:p.Tyr136=
NM_033164.4:c.374A=	NP_149354.1:p.Tyr125=
NM_033165.4:c.287A=	NP_149355.1:p.Tyr96=
NM_001206389.2:c.95A=	NP_001193318.1:p.Tyr32=
NM_006119.6:c.320A=	NP_006110.1:p.Tyr107=
NM_033163.5:c.407A= MANE Select	NP_149353.1:p.Tyr136=
NM_033165.5:c.287A=	NP_149355.1:p.Tyr96=