Canonical Allele Identifier: CA2578494280
Gene: FGFR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177091012del , CM000667.2:g.177091012del GRCh38
NC_000005.9:g.176518013del , CM000667.1:g.176518013del GRCh37
NC_000005.8:g.176450619del NCBI36
NG_012067.1:g.9093del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.511del MANE Select ENSP00000292408.4:p.Arg171AlafsTer?
ENST00000292408.8:c.511del ENSP00000292408.4:p.Arg171AlafsTer?
ENST00000393637.5:c.511del ENSP00000377254.1:p.Arg171AlafsTer?
ENST00000393648.6:c.511del ENSP00000377259.2:p.Arg171AlafsTer?
ENST00000426612.5:n.628del
ENST00000430285.5:c.*375del ENSP00000395164.1:n.*375del
ENST00000502906.5:c.511del ENSP00000424960.1:p.Arg171AlafsTer?
ENST00000503708.5:c.511del ENSP00000424905.1:p.Arg171AlafsTer?
ENST00000509511.5:n.511del
NM_001291980.1:c.511del NP_001278909.1:p.Arg171AlafsTer?
NM_002011.4:c.511del NP_002002.3:p.Arg171AlafsTer?
NM_022963.3:c.511del NP_075252.2:p.Arg171AlafsTer?
NM_213647.2:c.511del NP_998812.1:p.Arg171AlafsTer?
XM_005265838.2:c.511del XP_005265895.1:p.Arg171AlafsTer?
XM_011534464.1:c.604del XP_011532766.1:p.Arg202AlafsTer?
XM_011534465.1:c.193del XP_011532767.1:p.Arg65AlafsTer?
XR_941090.1:n.556del
NM_001354984.1:c.511del NP_001341913.1:p.Arg171AlafsTer?
NM_213647.3:c.511del MANE Select NP_998812.1:p.Arg171AlafsTer?
NM_001291980.2:c.511del NP_001278909.1:p.Arg171AlafsTer?
NM_001354984.2:c.511del NP_001341913.1:p.Arg171AlafsTer?
NM_002011.5:c.511del NP_002002.3:p.Arg171AlafsTer?