Canonical Allele Identifier: CA2610620521
Gene: FGF8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101775069_101775070insATCCCC , CM000672.2:g.101775069_101775070insATCCCC GRCh38
NC_000010.10:g.103534826_103534827insATCCCC , CM000672.1:g.103534826_103534827insATCCCC GRCh37
NC_000010.9:g.103524816_103524817insATCCCC NCBI36
NG_007151.1:g.6003_6004insGGATGG

Transcript Alleles

HGVS Amino-acid change
ENST00000320185.7:c.156+62_156+63insGGATGG MANE Select ENSP00000321797.2:n.156+62_156+63insGGATG...
ENST00000618991.5:c.-123-189_-123-188insGGATGG ENSP00000484420.1:n.-123-189_-123-188insG...
ENST00000344255.8:c.156+62_156+63insGGATGG ENSP00000340039.3:n.156+62_156+63insGGATG...
ENST00000320185.6:c.156+62_156+63insGGATGG ENSP00000321797.2:n.156+62_156+63insGGATG...
ENST00000344255.7:c.156+62_156+63insGGATGG ENSP00000340039.3:n.156+62_156+63insGGATG...
ENST00000346714.7:c.70-189_70-188insGGATGG ENSP00000344306.3:n.70-189_70-188insGGATG...
ENST00000347978.2:c.70-156_70-155insGGATGG ENSP00000321945.2:n.70-156_70-155insGGATG...
ENST00000469792.6:c.*154-189_*154-188insGGATGG ENSP00000473299.1:n.*154-189_*154-188insG...
ENST00000485728.1:n.33-156_33-155insGGATGG
ENST00000618991.4:c.-123-189_-123-188insGGATGG ENSP00000484420.1:n.-123-189_-123-188insG...
NM_001206389.1:c.-123-189_-123-188insGGATGG NP_001193318.1:n.-123-189_-123-188insGGAT...
NM_006119.4:c.70-156_70-155insGGATGG NP_006110.1:n.70-156_70-155insGGATGG
NM_033163.3:c.156+62_156+63insGGATGG NP_149353.1:n.156+62_156+63insGGATGG
NM_033164.3:c.156+62_156+63insGGATGG NP_149354.1:n.156+62_156+63insGGATGG
NM_033165.3:c.70-189_70-188insGGATGG NP_149355.1:n.70-189_70-188insGGATGG
XM_011539509.1:c.79-156_79-155insGGATGG XP_011537811.1:n.79-156_79-155insGGATGG
NM_006119.5:c.70-156_70-155insGGATGG NP_006110.1:n.70-156_70-155insGGATGG
NM_033163.4:c.156+62_156+63insGGATGG NP_149353.1:n.156+62_156+63insGGATGG
NM_033164.4:c.156+62_156+63insGGATGG NP_149354.1:n.156+62_156+63insGGATGG
NM_033165.4:c.70-189_70-188insGGATGG NP_149355.1:n.70-189_70-188insGGATGG
NM_001206389.2:c.-123-189_-123-188insGGATGG NP_001193318.1:n.-123-189_-123-188insGGAT...
NM_006119.6:c.70-156_70-155insGGATGG NP_006110.1:n.70-156_70-155insGGATGG
NM_033163.5:c.156+62_156+63insGGATGG MANE Select NP_149353.1:n.156+62_156+63insGGATGG
NM_033165.5:c.70-189_70-188insGGATGG NP_149355.1:n.70-189_70-188insGGATGG