Canonical Allele Identifier: CA362286867
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs1255439106

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177090961C>A , CM000667.2:g.177090961C>A GRCh38
NC_000005.9:g.176517962C>A , CM000667.1:g.176517962C>A GRCh37
NC_000005.8:g.176450568C>A NCBI36
NG_012067.1:g.9042C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.460C>A MANE Select ENSP00000292408.4:p.Arg154Ser
ENST00000292408.8:c.460C>A ENSP00000292408.4:p.Arg154Ser
ENST00000393637.5:c.460C>A ENSP00000377254.1:p.Arg154Ser
ENST00000393648.6:c.460C>A ENSP00000377259.2:p.Arg154Ser
ENST00000426612.5:n.577C>A
ENST00000430285.5:c.*324C>A ENSP00000395164.1:n.*324C>A
ENST00000502906.5:c.460C>A ENSP00000424960.1:p.Arg154Ser
ENST00000503708.5:c.460C>A ENSP00000424905.1:p.Arg154Ser
ENST00000509511.5:n.460C>A
NM_001291980.1:c.460C>A NP_001278909.1:p.Arg154Ser
NM_002011.4:c.460C>A NP_002002.3:p.Arg154Ser
NM_022963.3:c.460C>A NP_075252.2:p.Arg154Ser
NM_213647.2:c.460C>A NP_998812.1:p.Arg154Ser
XM_005265838.2:c.460C>A XP_005265895.1:p.Arg154Ser
XM_011534464.1:c.553C>A XP_011532766.1:p.Arg185Ser
XM_011534465.1:c.142C>A XP_011532767.1:p.Arg48Ser
XR_941090.1:n.505C>A
NM_001354984.1:c.460C>A NP_001341913.1:p.Arg154Ser
NM_213647.3:c.460C>A MANE Select NP_998812.1:p.Arg154Ser
NM_001291980.2:c.460C>A NP_001278909.1:p.Arg154Ser
NM_001354984.2:c.460C>A NP_001341913.1:p.Arg154Ser
NM_002011.5:c.460C>A NP_002002.3:p.Arg154Ser