Canonical Allele Identifier: CA377834439

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531281A>T (hg19) ; chr10:g.101771524A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771524A>T , CM000672.2:g.101771524A>T	GRCh38
NC_000010.10:g.103531281A>T , CM000672.1:g.103531281A>T	GRCh37
NC_000010.9:g.103521271A>T	NCBI36
NG_007151.1:g.9547T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.383T>A MANE Select	ENSP00000321797.2:p.Val128Asp
ENST00000618991.5:c.71T>A	ENSP00000484420.1:p.Val24Asp
ENST00000344255.8:c.350T>A	ENSP00000340039.3:p.Val117Asp
ENST00000320185.6:c.383T>A	ENSP00000321797.2:p.Val128Asp
ENST00000344255.7:c.350T>A	ENSP00000340039.3:p.Val117Asp
ENST00000346714.7:c.263T>A	ENSP00000344306.3:p.Val88Asp
ENST00000347978.2:c.296T>A	ENSP00000321945.2:p.Val99Asp
ENST00000469792.6:c.*347T>A	ENSP00000473299.1:n.*347T>A
ENST00000485728.1:n.259T>A
ENST00000618991.4:c.71T>A	ENSP00000484420.1:p.Val24Asp
NM_001206389.1:c.71T>A	NP_001193318.1:p.Val24Asp
NM_006119.4:c.296T>A	NP_006110.1:p.Val99Asp
NM_033163.3:c.383T>A	NP_149353.1:p.Val128Asp
NM_033164.3:c.350T>A	NP_149354.1:p.Val117Asp
NM_033165.3:c.263T>A	NP_149355.1:p.Val88Asp
XM_011539509.1:c.305T>A	XP_011537811.1:p.Val102Asp
XR_946251.1:n.305A>T
XR_946252.1:n.236A>T
XR_946253.1:n.234A>T
XR_946252.2:n.326A>T
XR_946253.2:n.324A>T
NM_006119.5:c.296T>A	NP_006110.1:p.Val99Asp
NM_033163.4:c.383T>A	NP_149353.1:p.Val128Asp
NM_033164.4:c.350T>A	NP_149354.1:p.Val117Asp
NM_033165.4:c.263T>A	NP_149355.1:p.Val88Asp
NM_001206389.2:c.71T>A	NP_001193318.1:p.Val24Asp
NM_006119.6:c.296T>A	NP_006110.1:p.Val99Asp
NM_033163.5:c.383T>A MANE Select	NP_149353.1:p.Val128Asp
NM_033165.5:c.263T>A	NP_149355.1:p.Val88Asp