Canonical Allele Identifier: CA377836199

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534506T>A (hg19) ; chr10:g.101774749T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774749T>A , CM000672.2:g.101774749T>A	GRCh38
NC_000010.10:g.103534506T>A , CM000672.1:g.103534506T>A	GRCh37
NC_000010.9:g.103524496T>A	NCBI36
NG_007151.1:g.6322A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.320A>T MANE Select	ENSP00000321797.2:p.Glu107Val
ENST00000618991.5:c.8A>T	ENSP00000484420.1:p.Glu3Val
ENST00000344255.8:c.287A>T	ENSP00000340039.3:p.Glu96Val
ENST00000320185.6:c.320A>T	ENSP00000321797.2:p.Glu107Val
ENST00000344255.7:c.287A>T	ENSP00000340039.3:p.Glu96Val
ENST00000346714.7:c.200A>T	ENSP00000344306.3:p.Glu67Val
ENST00000347978.2:c.233A>T	ENSP00000321945.2:p.Glu78Val
ENST00000469792.6:c.*284A>T	ENSP00000473299.1:n.*284A>T
ENST00000485728.1:n.196A>T
ENST00000618991.4:c.8A>T	ENSP00000484420.1:p.Glu3Val
NM_001206389.1:c.8A>T	NP_001193318.1:p.Glu3Val
NM_006119.4:c.233A>T	NP_006110.1:p.Glu78Val
NM_033163.3:c.320A>T	NP_149353.1:p.Glu107Val
NM_033164.3:c.287A>T	NP_149354.1:p.Glu96Val
NM_033165.3:c.200A>T	NP_149355.1:p.Glu67Val
XM_011539509.1:c.242A>T	XP_011537811.1:p.Glu81Val
NM_006119.5:c.233A>T	NP_006110.1:p.Glu78Val
NM_033163.4:c.320A>T	NP_149353.1:p.Glu107Val
NM_033164.4:c.287A>T	NP_149354.1:p.Glu96Val
NM_033165.4:c.200A>T	NP_149355.1:p.Glu67Val
NM_001206389.2:c.8A>T	NP_001193318.1:p.Glu3Val
NM_006119.6:c.233A>T	NP_006110.1:p.Glu78Val
NM_033163.5:c.320A>T MANE Select	NP_149353.1:p.Glu107Val
NM_033165.5:c.200A>T	NP_149355.1:p.Glu67Val