Canonical Allele Identifier: CA917647795
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs1562072240

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093535del , CM000667.2:g.177093535del GRCh38
NC_000005.9:g.176520536del , CM000667.1:g.176520536del GRCh37
NC_000005.8:g.176453142del NCBI36
NG_012067.1:g.11616del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1381del MANE Select ENSP00000292408.4:p.Glu461SerfsTer13
ENST00000292408.8:c.1381del ENSP00000292408.4:p.Glu461SerfsTer13
ENST00000393637.5:c.1261del ENSP00000377254.1:p.Glu421SerfsTer13
ENST00000393648.6:c.1193+34del ENSP00000377259.2:n.1193+34del
ENST00000502906.5:c.1381del ENSP00000424960.1:p.Glu461SerfsTer13
ENST00000511076.1:c.275del
NM_001291980.1:c.1193+34del NP_001278909.1:n.1193+34del
NM_002011.4:c.1381del NP_002002.3:p.Glu461SerfsTer13
NM_022963.3:c.1261del NP_075252.2:p.Glu421SerfsTer13
NM_213647.2:c.1381del NP_998812.1:p.Glu461SerfsTer13
XM_005265838.2:c.1381del XP_005265895.1:p.Glu461SerfsTer13
XM_011534464.1:c.1474del XP_011532766.1:p.Glu492SerfsTer13
XM_011534465.1:c.1063del XP_011532767.1:p.Glu355SerfsTer13
XR_941090.1:n.1392+34del
NM_001354984.1:c.1381del NP_001341913.1:p.Glu461SerfsTer13
NM_213647.3:c.1381del MANE Select NP_998812.1:p.Glu461SerfsTer13
NM_001291980.2:c.1193+34del NP_001278909.1:n.1193+34del
NM_001354984.2:c.1381del NP_001341913.1:p.Glu461SerfsTer13
NM_002011.5:c.1381del NP_002002.3:p.Glu461SerfsTer13