Canonical Allele Identifier: CA362286520
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs2149731291

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177090747T>A , CM000667.2:g.177090747T>A GRCh38
NC_000005.9:g.176517748T>A , CM000667.1:g.176517748T>A GRCh37
NC_000005.8:g.176450354T>A NCBI36
NG_012067.1:g.8828T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.358T>A MANE Select ENSP00000292408.4:p.Ser120Thr
ENST00000292408.8:c.358T>A ENSP00000292408.4:p.Ser120Thr
ENST00000393637.5:c.358T>A ENSP00000377254.1:p.Ser120Thr
ENST00000393648.6:c.358T>A ENSP00000377259.2:p.Ser120Thr
ENST00000426612.5:n.363T>A
ENST00000430285.5:c.*222T>A ENSP00000395164.1:n.*222T>A
ENST00000502906.5:c.358T>A ENSP00000424960.1:p.Ser120Thr
ENST00000503708.5:c.358T>A ENSP00000424905.1:p.Ser120Thr
ENST00000509511.5:n.358T>A
NM_001291980.1:c.358T>A NP_001278909.1:p.Ser120Thr
NM_002011.4:c.358T>A NP_002002.3:p.Ser120Thr
NM_022963.3:c.358T>A NP_075252.2:p.Ser120Thr
NM_213647.2:c.358T>A NP_998812.1:p.Ser120Thr
XM_005265838.2:c.358T>A XP_005265895.1:p.Ser120Thr
XM_011534464.1:c.451T>A XP_011532766.1:p.Ser151Thr
XM_011534465.1:c.40T>A XP_011532767.1:p.Ser14Thr
XR_941090.1:n.403T>A
NM_001354984.1:c.358T>A NP_001341913.1:p.Ser120Thr
NM_213647.3:c.358T>A MANE Select NP_998812.1:p.Ser120Thr
NM_001291980.2:c.358T>A NP_001278909.1:p.Ser120Thr
NM_001354984.2:c.358T>A NP_001341913.1:p.Ser120Thr
NM_002011.5:c.358T>A NP_002002.3:p.Ser120Thr