Canonical Allele Identifier: CA362290264
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177092784G>T , CM000667.2:g.177092784G>T GRCh38
NC_000005.9:g.176519785G>T , CM000667.1:g.176519785G>T GRCh37
NC_000005.8:g.176452391G>T NCBI36
NG_012067.1:g.10865G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1057G>T MANE Select ENSP00000292408.4:p.Glu353Ter
ENST00000292408.8:c.1057G>T ENSP00000292408.4:p.Glu353Ter
ENST00000393637.5:c.1057G>T ENSP00000377254.1:p.Gly353Cys
ENST00000393648.6:c.1057G>T ENSP00000377259.2:p.Glu353Ter
ENST00000502906.5:c.1057G>T ENSP00000424960.1:p.Glu353Ter
ENST00000508139.1:n.361G>T
ENST00000509511.5:n.1057G>T
NM_001291980.1:c.1057G>T NP_001278909.1:p.Glu353Ter
NM_002011.4:c.1057G>T NP_002002.3:p.Glu353Ter
NM_022963.3:c.1057G>T NP_075252.2:p.Gly353Cys
NM_213647.2:c.1057G>T NP_998812.1:p.Glu353Ter
XM_005265838.2:c.1057G>T XP_005265895.1:p.Glu353Ter
XM_011534464.1:c.1150G>T XP_011532766.1:p.Glu384Ter
XM_011534465.1:c.739G>T XP_011532767.1:p.Glu247Ter
XR_941090.1:n.1102G>T
NM_001354984.1:c.1057G>T NP_001341913.1:p.Glu353Ter
NM_213647.3:c.1057G>T MANE Select NP_998812.1:p.Glu353Ter
NM_001291980.2:c.1057G>T NP_001278909.1:p.Glu353Ter
NM_001354984.2:c.1057G>T NP_001341913.1:p.Glu353Ter
NM_002011.5:c.1057G>T NP_002002.3:p.Glu353Ter