Canonical Allele Identifier: CA1603397458
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs1784446005

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093544del , CM000667.2:g.177093544del GRCh38
NC_000005.9:g.176520545del , CM000667.1:g.176520545del GRCh37
NC_000005.8:g.176453151del NCBI36
NG_012067.1:g.11625del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1390del MANE Select ENSP00000292408.4:p.Arg464GlyfsTer10
ENST00000292408.8:c.1390del ENSP00000292408.4:p.Arg464GlyfsTer10
ENST00000393637.5:c.1270del ENSP00000377254.1:p.Arg424GlyfsTer10
ENST00000393648.6:c.1193+43del ENSP00000377259.2:n.1193+43del
ENST00000502906.5:c.1390del ENSP00000424960.1:p.Arg464GlyfsTer10
ENST00000511076.1:c.284del
NM_001291980.1:c.1193+43del NP_001278909.1:n.1193+43del
NM_002011.4:c.1390del NP_002002.3:p.Arg464GlyfsTer10
NM_022963.3:c.1270del NP_075252.2:p.Arg424GlyfsTer10
NM_213647.2:c.1390del NP_998812.1:p.Arg464GlyfsTer10
XM_005265838.2:c.1390del XP_005265895.1:p.Arg464GlyfsTer10
XM_011534464.1:c.1483del XP_011532766.1:p.Arg495GlyfsTer10
XM_011534465.1:c.1072del XP_011532767.1:p.Arg358GlyfsTer10
XR_941090.1:n.1392+43del
NM_001354984.1:c.1390del NP_001341913.1:p.Arg464GlyfsTer10
NM_213647.3:c.1390del MANE Select NP_998812.1:p.Arg464GlyfsTer10
NM_001291980.2:c.1193+43del NP_001278909.1:n.1193+43del
NM_001354984.2:c.1390del NP_001341913.1:p.Arg464GlyfsTer10
NM_002011.5:c.1390del NP_002002.3:p.Arg464GlyfsTer10