Canonical Allele Identifier: CA377836222

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534510C>T (hg19) ; chr10:g.101774753C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774753C>T , CM000672.2:g.101774753C>T	GRCh38
NC_000010.10:g.103534510C>T , CM000672.1:g.103534510C>T	GRCh37
NC_000010.9:g.103524500C>T	NCBI36
NG_007151.1:g.6318G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.316G>A MANE Select	ENSP00000321797.2:p.Ala106Thr
ENST00000618991.5:c.4G>A	ENSP00000484420.1:p.Ala2Thr
ENST00000344255.8:c.283G>A	ENSP00000340039.3:p.Ala95Thr
ENST00000320185.6:c.316G>A	ENSP00000321797.2:p.Ala106Thr
ENST00000344255.7:c.283G>A	ENSP00000340039.3:p.Ala95Thr
ENST00000346714.7:c.196G>A	ENSP00000344306.3:p.Ala66Thr
ENST00000347978.2:c.229G>A	ENSP00000321945.2:p.Ala77Thr
ENST00000469792.6:c.*280G>A	ENSP00000473299.1:n.*280G>A
ENST00000485728.1:n.192G>A
ENST00000618991.4:c.4G>A	ENSP00000484420.1:p.Ala2Thr
NM_001206389.1:c.4G>A	NP_001193318.1:p.Ala2Thr
NM_006119.4:c.229G>A	NP_006110.1:p.Ala77Thr
NM_033163.3:c.316G>A	NP_149353.1:p.Ala106Thr
NM_033164.3:c.283G>A	NP_149354.1:p.Ala95Thr
NM_033165.3:c.196G>A	NP_149355.1:p.Ala66Thr
XM_011539509.1:c.238G>A	XP_011537811.1:p.Ala80Thr
NM_006119.5:c.229G>A	NP_006110.1:p.Ala77Thr
NM_033163.4:c.316G>A	NP_149353.1:p.Ala106Thr
NM_033164.4:c.283G>A	NP_149354.1:p.Ala95Thr
NM_033165.4:c.196G>A	NP_149355.1:p.Ala66Thr
NM_001206389.2:c.4G>A	NP_001193318.1:p.Ala2Thr
NM_006119.6:c.229G>A	NP_006110.1:p.Ala77Thr
NM_033163.5:c.316G>A MANE Select	NP_149353.1:p.Ala106Thr
NM_033165.5:c.196G>A	NP_149355.1:p.Ala66Thr