Canonical Allele Identifier: CA377834499

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531299A>G (hg19) ; chr10:g.101771542A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771542A>G , CM000672.2:g.101771542A>G	GRCh38
NC_000010.10:g.103531299A>G , CM000672.1:g.103531299A>G	GRCh37
NC_000010.9:g.103521289A>G	NCBI36
NG_007151.1:g.9529T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.365T>C MANE Select	ENSP00000321797.2:p.Phe122Ser
ENST00000618991.5:c.53T>C	ENSP00000484420.1:p.Phe18Ser
ENST00000344255.8:c.332T>C	ENSP00000340039.3:p.Phe111Ser
ENST00000320185.6:c.365T>C	ENSP00000321797.2:p.Phe122Ser
ENST00000344255.7:c.332T>C	ENSP00000340039.3:p.Phe111Ser
ENST00000346714.7:c.245T>C	ENSP00000344306.3:p.Phe82Ser
ENST00000347978.2:c.278T>C	ENSP00000321945.2:p.Phe93Ser
ENST00000469792.6:c.*329T>C	ENSP00000473299.1:n.*329T>C
ENST00000485728.1:n.241T>C
ENST00000618991.4:c.53T>C	ENSP00000484420.1:p.Phe18Ser
NM_001206389.1:c.53T>C	NP_001193318.1:p.Phe18Ser
NM_006119.4:c.278T>C	NP_006110.1:p.Phe93Ser
NM_033163.3:c.365T>C	NP_149353.1:p.Phe122Ser
NM_033164.3:c.332T>C	NP_149354.1:p.Phe111Ser
NM_033165.3:c.245T>C	NP_149355.1:p.Phe82Ser
XM_011539509.1:c.287T>C	XP_011537811.1:p.Phe96Ser
XR_946251.1:n.323A>G
XR_946252.1:n.254A>G
XR_946253.1:n.252A>G
XR_946252.2:n.344A>G
XR_946253.2:n.342A>G
NM_006119.5:c.278T>C	NP_006110.1:p.Phe93Ser
NM_033163.4:c.365T>C	NP_149353.1:p.Phe122Ser
NM_033164.4:c.332T>C	NP_149354.1:p.Phe111Ser
NM_033165.4:c.245T>C	NP_149355.1:p.Phe82Ser
NM_001206389.2:c.53T>C	NP_001193318.1:p.Phe18Ser
NM_006119.6:c.278T>C	NP_006110.1:p.Phe93Ser
NM_033163.5:c.365T>C MANE Select	NP_149353.1:p.Phe122Ser
NM_033165.5:c.245T>C	NP_149355.1:p.Phe82Ser