Canonical Allele Identifier: CA2676680988
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177090812_177090821del , CM000667.2:g.177090812_177090821del GRCh38
NC_000005.9:g.176517813_176517822del , CM000667.1:g.176517813_176517822del GRCh37
NC_000005.8:g.176450419_176450428del NCBI36
NG_012067.1:g.8893_8902del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.423_432del MANE Select ENSP00000292408.4:p.Tyr142LysfsTer?
ENST00000292408.8:c.423_432del ENSP00000292408.4:p.Tyr142LysfsTer?
ENST00000393637.5:c.423_432del ENSP00000377254.1:p.Tyr142LysfsTer?
ENST00000393648.6:c.423_432del ENSP00000377259.2:p.Tyr142LysfsTer?
ENST00000426612.5:n.428_437del
ENST00000430285.5:c.*287_*296del ENSP00000395164.1:n.*287_*296del
ENST00000502906.5:c.423_432del ENSP00000424960.1:p.Tyr142LysfsTer?
ENST00000503708.5:c.423_432del ENSP00000424905.1:p.Tyr142LysfsTer?
ENST00000509511.5:n.423_432del
NM_001291980.1:c.423_432del NP_001278909.1:p.Tyr142LysfsTer?
NM_002011.4:c.423_432del NP_002002.3:p.Tyr142LysfsTer?
NM_022963.3:c.423_432del NP_075252.2:p.Tyr142LysfsTer?
NM_213647.2:c.423_432del NP_998812.1:p.Tyr142LysfsTer?
XM_005265838.2:c.423_432del XP_005265895.1:p.Tyr142LysfsTer?
XM_011534464.1:c.516_525del XP_011532766.1:p.Tyr173LysfsTer?
XM_011534465.1:c.105_114del XP_011532767.1:p.Tyr36LysfsTer?
XR_941090.1:n.468_477del
NM_001354984.1:c.423_432del NP_001341913.1:p.Tyr142LysfsTer?
NM_213647.3:c.423_432del MANE Select NP_998812.1:p.Tyr142LysfsTer?
NM_001291980.2:c.423_432del NP_001278909.1:p.Tyr142LysfsTer?
NM_001354984.2:c.423_432del NP_001341913.1:p.Tyr142LysfsTer?
NM_002011.5:c.423_432del NP_002002.3:p.Tyr142LysfsTer?