Canonical Allele Identifier: CA377834342

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531252A>T (hg19) ; chr10:g.101771495A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771495A>T , CM000672.2:g.101771495A>T	GRCh38
NC_000010.10:g.103531252A>T , CM000672.1:g.103531252A>T	GRCh37
NC_000010.9:g.103521242A>T	NCBI36
NG_007151.1:g.9576T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.412T>A MANE Select	ENSP00000321797.2:p.Cys138Ser
ENST00000618991.5:c.100T>A	ENSP00000484420.1:p.Cys34Ser
ENST00000344255.8:c.379T>A	ENSP00000340039.3:p.Cys127Ser
ENST00000320185.6:c.412T>A	ENSP00000321797.2:p.Cys138Ser
ENST00000344255.7:c.379T>A	ENSP00000340039.3:p.Cys127Ser
ENST00000346714.7:c.292T>A	ENSP00000344306.3:p.Cys98Ser
ENST00000347978.2:c.325T>A	ENSP00000321945.2:p.Cys109Ser
ENST00000469792.6:c.*376T>A	ENSP00000473299.1:n.*376T>A
ENST00000485728.1:n.288T>A
ENST00000618991.4:c.100T>A	ENSP00000484420.1:p.Cys34Ser
NM_001206389.1:c.100T>A	NP_001193318.1:p.Cys34Ser
NM_006119.4:c.325T>A	NP_006110.1:p.Cys109Ser
NM_033163.3:c.412T>A	NP_149353.1:p.Cys138Ser
NM_033164.3:c.379T>A	NP_149354.1:p.Cys127Ser
NM_033165.3:c.292T>A	NP_149355.1:p.Cys98Ser
XM_011539509.1:c.334T>A	XP_011537811.1:p.Cys112Ser
XR_946251.1:n.278-2A>T
XR_946252.1:n.209-2A>T
XR_946253.1:n.207-2A>T
XR_946252.2:n.299-2A>T
XR_946253.2:n.297-2A>T
NM_006119.5:c.325T>A	NP_006110.1:p.Cys109Ser
NM_033163.4:c.412T>A	NP_149353.1:p.Cys138Ser
NM_033164.4:c.379T>A	NP_149354.1:p.Cys127Ser
NM_033165.4:c.292T>A	NP_149355.1:p.Cys98Ser
NM_001206389.2:c.100T>A	NP_001193318.1:p.Cys34Ser
NM_006119.6:c.325T>A	NP_006110.1:p.Cys109Ser
NM_033163.5:c.412T>A MANE Select	NP_149353.1:p.Cys138Ser
NM_033165.5:c.292T>A	NP_149355.1:p.Cys98Ser