Canonical Allele Identifier: CA377834440

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531282C>A (hg19) ; chr10:g.101771525C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771525C>A , CM000672.2:g.101771525C>A	GRCh38
NC_000010.10:g.103531282C>A , CM000672.1:g.103531282C>A	GRCh37
NC_000010.9:g.103521272C>A	NCBI36
NG_007151.1:g.9546G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.382G>T MANE Select	ENSP00000321797.2:p.Val128Phe
ENST00000618991.5:c.70G>T	ENSP00000484420.1:p.Val24Phe
ENST00000344255.8:c.349G>T	ENSP00000340039.3:p.Val117Phe
ENST00000320185.6:c.382G>T	ENSP00000321797.2:p.Val128Phe
ENST00000344255.7:c.349G>T	ENSP00000340039.3:p.Val117Phe
ENST00000346714.7:c.262G>T	ENSP00000344306.3:p.Val88Phe
ENST00000347978.2:c.295G>T	ENSP00000321945.2:p.Val99Phe
ENST00000469792.6:c.*346G>T	ENSP00000473299.1:n.*346G>T
ENST00000485728.1:n.258G>T
ENST00000618991.4:c.70G>T	ENSP00000484420.1:p.Val24Phe
NM_001206389.1:c.70G>T	NP_001193318.1:p.Val24Phe
NM_006119.4:c.295G>T	NP_006110.1:p.Val99Phe
NM_033163.3:c.382G>T	NP_149353.1:p.Val128Phe
NM_033164.3:c.349G>T	NP_149354.1:p.Val117Phe
NM_033165.3:c.262G>T	NP_149355.1:p.Val88Phe
XM_011539509.1:c.304G>T	XP_011537811.1:p.Val102Phe
XR_946251.1:n.306C>A
XR_946252.1:n.237C>A
XR_946253.1:n.235C>A
XR_946252.2:n.327C>A
XR_946253.2:n.325C>A
NM_006119.5:c.295G>T	NP_006110.1:p.Val99Phe
NM_033163.4:c.382G>T	NP_149353.1:p.Val128Phe
NM_033164.4:c.349G>T	NP_149354.1:p.Val117Phe
NM_033165.4:c.262G>T	NP_149355.1:p.Val88Phe
NM_001206389.2:c.70G>T	NP_001193318.1:p.Val24Phe
NM_006119.6:c.295G>T	NP_006110.1:p.Val99Phe
NM_033163.5:c.382G>T MANE Select	NP_149353.1:p.Val128Phe
NM_033165.5:c.262G>T	NP_149355.1:p.Val88Phe