Canonical Allele Identifier: CA362291786
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs1562071377

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093273G>C , CM000667.2:g.177093273G>C GRCh38
NC_000005.9:g.176520274G>C , CM000667.1:g.176520274G>C GRCh37
NC_000005.8:g.176452880G>C NCBI36
NG_012067.1:g.11354G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1193G>C MANE Select ENSP00000292408.4:p.Arg398Pro
ENST00000292408.8:c.1193G>C ENSP00000292408.4:p.Arg398Pro
ENST00000393637.5:c.1058-59G>C ENSP00000377254.1:n.1058-59G>C
ENST00000393648.6:c.1097+96G>C ENSP00000377259.2:n.1097+96G>C
ENST00000502906.5:c.1193G>C ENSP00000424960.1:p.Arg398Pro
ENST00000508139.1:n.497G>C
ENST00000511076.1:c.99G>C
NM_001291980.1:c.1097+96G>C NP_001278909.1:n.1097+96G>C
NM_002011.4:c.1193G>C NP_002002.3:p.Arg398Pro
NM_022963.3:c.1058-59G>C NP_075252.2:n.1058-59G>C
NM_213647.2:c.1193G>C NP_998812.1:p.Arg398Pro
XM_005265838.2:c.1193G>C XP_005265895.1:p.Arg398Pro
XM_011534464.1:c.1286G>C XP_011532766.1:p.Arg429Pro
XM_011534465.1:c.875G>C XP_011532767.1:p.Arg292Pro
XR_941090.1:n.1238G>C
NM_001354984.1:c.1193G>C NP_001341913.1:p.Arg398Pro
NM_213647.3:c.1193G>C MANE Select NP_998812.1:p.Arg398Pro
NM_001291980.2:c.1097+96G>C NP_001278909.1:n.1097+96G>C
NM_001354984.2:c.1193G>C NP_001341913.1:p.Arg398Pro
NM_002011.5:c.1193G>C NP_002002.3:p.Arg398Pro