Canonical Allele Identifier: CA132827618
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs996490269

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177090950C>G , CM000667.2:g.177090950C>G GRCh38
NC_000005.9:g.176517951C>G , CM000667.1:g.176517951C>G GRCh37
NC_000005.8:g.176450557C>G NCBI36
NG_012067.1:g.9031C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.449C>G MANE Select ENSP00000292408.4:p.Thr150Arg
ENST00000292408.8:c.449C>G ENSP00000292408.4:p.Thr150Arg
ENST00000393637.5:c.449C>G ENSP00000377254.1:p.Thr150Arg
ENST00000393648.6:c.449C>G ENSP00000377259.2:p.Thr150Arg
ENST00000426612.5:n.566C>G
ENST00000430285.5:c.*313C>G ENSP00000395164.1:n.*313C>G
ENST00000502906.5:c.449C>G ENSP00000424960.1:p.Thr150Arg
ENST00000503708.5:c.449C>G ENSP00000424905.1:p.Thr150Arg
ENST00000509511.5:n.449C>G
NM_001291980.1:c.449C>G NP_001278909.1:p.Thr150Arg
NM_002011.4:c.449C>G NP_002002.3:p.Thr150Arg
NM_022963.3:c.449C>G NP_075252.2:p.Thr150Arg
NM_213647.2:c.449C>G NP_998812.1:p.Thr150Arg
XM_005265838.2:c.449C>G XP_005265895.1:p.Thr150Arg
XM_011534464.1:c.542C>G XP_011532766.1:p.Thr181Arg
XM_011534465.1:c.131C>G XP_011532767.1:p.Thr44Arg
XR_941090.1:n.494C>G
NM_001354984.1:c.449C>G NP_001341913.1:p.Thr150Arg
NM_213647.3:c.449C>G MANE Select NP_998812.1:p.Thr150Arg
NM_001291980.2:c.449C>G NP_001278909.1:p.Thr150Arg
NM_001354984.2:c.449C>G NP_001341913.1:p.Thr150Arg
NM_002011.5:c.449C>G NP_002002.3:p.Thr150Arg