Canonical Allele Identifier: CA2676681032
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177091025del , CM000667.2:g.177091025del GRCh38
NC_000005.9:g.176518026del , CM000667.1:g.176518026del GRCh37
NC_000005.8:g.176450632del NCBI36
NG_012067.1:g.9106del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.524del MANE Select ENSP00000292408.4:p.Ala175GlufsTer?
ENST00000292408.8:c.524del ENSP00000292408.4:p.Ala175GlufsTer?
ENST00000393637.5:c.524del ENSP00000377254.1:p.Ala175GlufsTer?
ENST00000393648.6:c.524del ENSP00000377259.2:p.Ala175GlufsTer?
ENST00000426612.5:n.641del
ENST00000430285.5:c.*388del ENSP00000395164.1:n.*388del
ENST00000502906.5:c.524del ENSP00000424960.1:p.Ala175GlufsTer?
ENST00000503708.5:c.524del ENSP00000424905.1:p.Ala175GlufsTer?
ENST00000509511.5:n.524del
NM_001291980.1:c.524del NP_001278909.1:p.Ala175GlufsTer?
NM_002011.4:c.524del NP_002002.3:p.Ala175GlufsTer?
NM_022963.3:c.524del NP_075252.2:p.Ala175GlufsTer?
NM_213647.2:c.524del NP_998812.1:p.Ala175GlufsTer?
XM_005265838.2:c.524del XP_005265895.1:p.Ala175GlufsTer?
XM_011534464.1:c.617del XP_011532766.1:p.Ala206GlufsTer?
XM_011534465.1:c.206del XP_011532767.1:p.Ala69GlufsTer?
XR_941090.1:n.569del
NM_001354984.1:c.524del NP_001341913.1:p.Ala175GlufsTer?
NM_213647.3:c.524del MANE Select NP_998812.1:p.Ala175GlufsTer?
NM_001291980.2:c.524del NP_001278909.1:p.Ala175GlufsTer?
NM_001354984.2:c.524del NP_001341913.1:p.Ala175GlufsTer?
NM_002011.5:c.524del NP_002002.3:p.Ala175GlufsTer?