Canonical Allele Identifier: CA1932376604

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774779A= , CM000672.2:g.101774779A=	GRCh38
NC_000010.10:g.103534536A= , CM000672.1:g.103534536A=	GRCh37
NC_000010.9:g.103524526A=	NCBI36
NG_007151.1:g.6292T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.290T= MANE Select	ENSP00000321797.2:p.Leu97=
ENST00000618991.5:c.-23T=	ENSP00000484420.1:n.-23T=
ENST00000344255.8:c.257T=	ENSP00000340039.3:p.Leu86=
ENST00000320185.6:c.290T=	ENSP00000321797.2:p.Leu97=
ENST00000344255.7:c.257T=	ENSP00000340039.3:p.Leu86=
ENST00000346714.7:c.170T=	ENSP00000344306.3:p.Leu57=
ENST00000347978.2:c.203T=	ENSP00000321945.2:p.Leu68=
ENST00000469792.6:c.*254T=	ENSP00000473299.1:n.*254T=
ENST00000485728.1:n.166T=
ENST00000618991.4:c.-23T=	ENSP00000484420.1:n.-23T=
NM_001206389.1:c.-23T=	NP_001193318.1:n.-23T=
NM_006119.4:c.203T=	NP_006110.1:p.Leu68=
NM_033163.3:c.290T=	NP_149353.1:p.Leu97=
NM_033164.3:c.257T=	NP_149354.1:p.Leu86=
NM_033165.3:c.170T=	NP_149355.1:p.Leu57=
XM_011539509.1:c.212T=	XP_011537811.1:p.Leu71=
NM_006119.5:c.203T=	NP_006110.1:p.Leu68=
NM_033163.4:c.290T=	NP_149353.1:p.Leu97=
NM_033164.4:c.257T=	NP_149354.1:p.Leu86=
NM_033165.4:c.170T=	NP_149355.1:p.Leu57=
NM_001206389.2:c.-23T=	NP_001193318.1:n.-23T=
NM_006119.6:c.203T=	NP_006110.1:p.Leu68=
NM_033163.5:c.290T= MANE Select	NP_149353.1:p.Leu97=
NM_033165.5:c.170T=	NP_149355.1:p.Leu57=