Canonical Allele Identifier: CA2676681604
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177092709_177092715del , CM000667.2:g.177092709_177092715del GRCh38
NC_000005.9:g.176519710_176519716del , CM000667.1:g.176519710_176519716del GRCh37
NC_000005.8:g.176452316_176452322del NCBI36
NG_012067.1:g.10790_10796del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.982_988del MANE Select ENSP00000292408.4:p.Ala328SerfsTer?
ENST00000292408.8:c.982_988del ENSP00000292408.4:p.Ala328SerfsTer?
ENST00000393637.5:c.982_988del ENSP00000377254.1:p.Ala328SerfsTer?
ENST00000393648.6:c.982_988del ENSP00000377259.2:p.Ala328SerfsTer?
ENST00000502906.5:c.982_988del ENSP00000424960.1:p.Ala328SerfsTer?
ENST00000508139.1:n.286_292del
ENST00000509511.5:n.982_988del
NM_001291980.1:c.982_988del NP_001278909.1:p.Ala328SerfsTer?
NM_002011.4:c.982_988del NP_002002.3:p.Ala328SerfsTer?
NM_022963.3:c.982_988del NP_075252.2:p.Ala328SerfsTer?
NM_213647.2:c.982_988del NP_998812.1:p.Ala328SerfsTer?
XM_005265838.2:c.982_988del XP_005265895.1:p.Ala328SerfsTer?
XM_011534464.1:c.1075_1081del XP_011532766.1:p.Ala359SerfsTer?
XM_011534465.1:c.664_670del XP_011532767.1:p.Ala222SerfsTer?
XR_941090.1:n.1027_1033del
NM_001354984.1:c.982_988del NP_001341913.1:p.Ala328SerfsTer?
NM_213647.3:c.982_988del MANE Select NP_998812.1:p.Ala328SerfsTer?
NM_001291980.2:c.982_988del NP_001278909.1:p.Ala328SerfsTer?
NM_001354984.2:c.982_988del NP_001341913.1:p.Ala328SerfsTer?
NM_002011.5:c.982_988del NP_002002.3:p.Ala328SerfsTer?