Canonical Allele Identifier: CA1932376749

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774836C= , CM000672.2:g.101774836C=	GRCh38
NC_000010.10:g.103534593C= , CM000672.1:g.103534593C=	GRCh37
NC_000010.9:g.103524583C=	NCBI36
NG_007151.1:g.6235G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.233G= MANE Select	ENSP00000321797.2:p.Arg78=
ENST00000618991.5:c.-80G=	ENSP00000484420.1:n.-80G=
ENST00000344255.8:c.200G=	ENSP00000340039.3:p.Arg67=
ENST00000320185.6:c.233G=	ENSP00000321797.2:p.Arg78=
ENST00000344255.7:c.200G=	ENSP00000340039.3:p.Arg67=
ENST00000346714.7:c.113G=	ENSP00000344306.3:p.Arg38=
ENST00000347978.2:c.146G=	ENSP00000321945.2:p.Arg49=
ENST00000469792.6:c.*197G=	ENSP00000473299.1:n.*197G=
ENST00000485728.1:n.109G=
ENST00000618991.4:c.-80G=	ENSP00000484420.1:n.-80G=
NM_001206389.1:c.-80G=	NP_001193318.1:n.-80G=
NM_006119.4:c.146G=	NP_006110.1:p.Arg49=
NM_033163.3:c.233G=	NP_149353.1:p.Arg78=
NM_033164.3:c.200G=	NP_149354.1:p.Arg67=
NM_033165.3:c.113G=	NP_149355.1:p.Arg38=
XM_011539509.1:c.155G=	XP_011537811.1:p.Arg52=
NM_006119.5:c.146G=	NP_006110.1:p.Arg49=
NM_033163.4:c.233G=	NP_149353.1:p.Arg78=
NM_033164.4:c.200G=	NP_149354.1:p.Arg67=
NM_033165.4:c.113G=	NP_149355.1:p.Arg38=
NM_001206389.2:c.-80G=	NP_001193318.1:n.-80G=
NM_006119.6:c.146G=	NP_006110.1:p.Arg49=
NM_033163.5:c.233G= MANE Select	NP_149353.1:p.Arg78=
NM_033165.5:c.113G=	NP_149355.1:p.Arg38=