Canonical Allele Identifier: CA377834502

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531300A>G (hg19) ; chr10:g.101771543A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771543A>G , CM000672.2:g.101771543A>G	GRCh38
NC_000010.10:g.103531300A>G , CM000672.1:g.103531300A>G	GRCh37
NC_000010.9:g.103521290A>G	NCBI36
NG_007151.1:g.9528T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.364T>C MANE Select	ENSP00000321797.2:p.Phe122Leu
ENST00000618991.5:c.52T>C	ENSP00000484420.1:p.Phe18Leu
ENST00000344255.8:c.331T>C	ENSP00000340039.3:p.Phe111Leu
ENST00000320185.6:c.364T>C	ENSP00000321797.2:p.Phe122Leu
ENST00000344255.7:c.331T>C	ENSP00000340039.3:p.Phe111Leu
ENST00000346714.7:c.244T>C	ENSP00000344306.3:p.Phe82Leu
ENST00000347978.2:c.277T>C	ENSP00000321945.2:p.Phe93Leu
ENST00000469792.6:c.*328T>C	ENSP00000473299.1:n.*328T>C
ENST00000485728.1:n.240T>C
ENST00000618991.4:c.52T>C	ENSP00000484420.1:p.Phe18Leu
NM_001206389.1:c.52T>C	NP_001193318.1:p.Phe18Leu
NM_006119.4:c.277T>C	NP_006110.1:p.Phe93Leu
NM_033163.3:c.364T>C	NP_149353.1:p.Phe122Leu
NM_033164.3:c.331T>C	NP_149354.1:p.Phe111Leu
NM_033165.3:c.244T>C	NP_149355.1:p.Phe82Leu
XM_011539509.1:c.286T>C	XP_011537811.1:p.Phe96Leu
XR_946251.1:n.324A>G
XR_946252.1:n.255A>G
XR_946253.1:n.253A>G
XR_946252.2:n.345A>G
XR_946253.2:n.343A>G
NM_006119.5:c.277T>C	NP_006110.1:p.Phe93Leu
NM_033163.4:c.364T>C	NP_149353.1:p.Phe122Leu
NM_033164.4:c.331T>C	NP_149354.1:p.Phe111Leu
NM_033165.4:c.244T>C	NP_149355.1:p.Phe82Leu
NM_001206389.2:c.52T>C	NP_001193318.1:p.Phe18Leu
NM_006119.6:c.277T>C	NP_006110.1:p.Phe93Leu
NM_033163.5:c.364T>C MANE Select	NP_149353.1:p.Phe122Leu
NM_033165.5:c.244T>C	NP_149355.1:p.Phe82Leu