Canonical Allele Identifier: CA377834348

Gene: FGF8

Linked Data

• COSMIC: COSM4616985
• MyVariant Identifiers: chr10:g.103531254A>G (hg19) ; chr10:g.101771497A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771497A>G , CM000672.2:g.101771497A>G	GRCh38
NC_000010.10:g.103531254A>G , CM000672.1:g.103531254A>G	GRCh37
NC_000010.9:g.103521244A>G	NCBI36
NG_007151.1:g.9574T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.410T>C MANE Select	ENSP00000321797.2:p.Ile137Thr
ENST00000618991.5:c.98T>C	ENSP00000484420.1:p.Ile33Thr
ENST00000344255.8:c.377T>C	ENSP00000340039.3:p.Ile126Thr
ENST00000320185.6:c.410T>C	ENSP00000321797.2:p.Ile137Thr
ENST00000344255.7:c.377T>C	ENSP00000340039.3:p.Ile126Thr
ENST00000346714.7:c.290T>C	ENSP00000344306.3:p.Ile97Thr
ENST00000347978.2:c.323T>C	ENSP00000321945.2:p.Ile108Thr
ENST00000469792.6:c.*374T>C	ENSP00000473299.1:n.*374T>C
ENST00000485728.1:n.286T>C
ENST00000618991.4:c.98T>C	ENSP00000484420.1:p.Ile33Thr
NM_001206389.1:c.98T>C	NP_001193318.1:p.Ile33Thr
NM_006119.4:c.323T>C	NP_006110.1:p.Ile108Thr
NM_033163.3:c.410T>C	NP_149353.1:p.Ile137Thr
NM_033164.3:c.377T>C	NP_149354.1:p.Ile126Thr
NM_033165.3:c.290T>C	NP_149355.1:p.Ile97Thr
XM_011539509.1:c.332T>C	XP_011537811.1:p.Ile111Thr
XR_946251.1:n.278A>G
XR_946252.1:n.209A>G
XR_946253.1:n.207A>G
XR_946252.2:n.299A>G
XR_946253.2:n.297A>G
NM_006119.5:c.323T>C	NP_006110.1:p.Ile108Thr
NM_033163.4:c.410T>C	NP_149353.1:p.Ile137Thr
NM_033164.4:c.377T>C	NP_149354.1:p.Ile126Thr
NM_033165.4:c.290T>C	NP_149355.1:p.Ile97Thr
NM_001206389.2:c.98T>C	NP_001193318.1:p.Ile33Thr
NM_006119.6:c.323T>C	NP_006110.1:p.Ile108Thr
NM_033163.5:c.410T>C MANE Select	NP_149353.1:p.Ile137Thr
NM_033165.5:c.290T>C	NP_149355.1:p.Ile97Thr