Canonical Allele Identifier: CA377836029
Gene: FGF8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101774732C>A , CM000672.2:g.101774732C>A GRCh38
NC_000010.10:g.103534489C>A , CM000672.1:g.103534489C>A GRCh37
NC_000010.9:g.103524479C>A NCBI36
NG_007151.1:g.6339G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320185.7:c.337G>T MANE Select ENSP00000321797.2:p.Ala113Ser
ENST00000618991.5:c.25G>T ENSP00000484420.1:p.Ala9Ser
ENST00000344255.8:c.304G>T ENSP00000340039.3:p.Ala102Ser
ENST00000320185.6:c.337G>T ENSP00000321797.2:p.Ala113Ser
ENST00000344255.7:c.304G>T ENSP00000340039.3:p.Ala102Ser
ENST00000346714.7:c.217G>T ENSP00000344306.3:p.Ala73Ser
ENST00000347978.2:c.250G>T ENSP00000321945.2:p.Ala84Ser
ENST00000469792.6:c.*301G>T ENSP00000473299.1:n.*301G>T
ENST00000485728.1:n.213G>T
ENST00000618991.4:c.25G>T ENSP00000484420.1:p.Ala9Ser
NM_001206389.1:c.25G>T NP_001193318.1:p.Ala9Ser
NM_006119.4:c.250G>T NP_006110.1:p.Ala84Ser
NM_033163.3:c.337G>T NP_149353.1:p.Ala113Ser
NM_033164.3:c.304G>T NP_149354.1:p.Ala102Ser
NM_033165.3:c.217G>T NP_149355.1:p.Ala73Ser
XM_011539509.1:c.259G>T XP_011537811.1:p.Ala87Ser
NM_006119.5:c.250G>T NP_006110.1:p.Ala84Ser
NM_033163.4:c.337G>T NP_149353.1:p.Ala113Ser
NM_033164.4:c.304G>T NP_149354.1:p.Ala102Ser
NM_033165.4:c.217G>T NP_149355.1:p.Ala73Ser
NM_001206389.2:c.25G>T NP_001193318.1:p.Ala9Ser
NM_006119.6:c.250G>T NP_006110.1:p.Ala84Ser
NM_033163.5:c.337G>T MANE Select NP_149353.1:p.Ala113Ser
NM_033165.5:c.217G>T NP_149355.1:p.Ala73Ser