Canonical Allele Identifier: CA2676681609
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177092741del , CM000667.2:g.177092741del GRCh38
NC_000005.9:g.176519742del , CM000667.1:g.176519742del GRCh37
NC_000005.8:g.176452348del NCBI36
NG_012067.1:g.10822del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1014del MANE Select ENSP00000292408.4:p.Ile339SerfsTer?
ENST00000292408.8:c.1014del ENSP00000292408.4:p.Ile339SerfsTer?
ENST00000393637.5:c.1014del ENSP00000377254.1:p.Ile339SerfsTer27
ENST00000393648.6:c.1014del ENSP00000377259.2:p.Ile339SerfsTer?
ENST00000502906.5:c.1014del ENSP00000424960.1:p.Ile339SerfsTer?
ENST00000508139.1:n.318del
ENST00000509511.5:n.1014del
NM_001291980.1:c.1014del NP_001278909.1:p.Ile339SerfsTer?
NM_002011.4:c.1014del NP_002002.3:p.Ile339SerfsTer?
NM_022963.3:c.1014del NP_075252.2:p.Ile339SerfsTer27
NM_213647.2:c.1014del NP_998812.1:p.Ile339SerfsTer?
XM_005265838.2:c.1014del XP_005265895.1:p.Ile339SerfsTer?
XM_011534464.1:c.1107del XP_011532766.1:p.Ile370SerfsTer?
XM_011534465.1:c.696del XP_011532767.1:p.Ile233SerfsTer?
XR_941090.1:n.1059del
NM_001354984.1:c.1014del NP_001341913.1:p.Ile339SerfsTer?
NM_213647.3:c.1014del MANE Select NP_998812.1:p.Ile339SerfsTer?
NM_001291980.2:c.1014del NP_001278909.1:p.Ile339SerfsTer?
NM_001354984.2:c.1014del NP_001341913.1:p.Ile339SerfsTer?
NM_002011.5:c.1014del NP_002002.3:p.Ile339SerfsTer?