Canonical Allele Identifier: CA2984983436
Gene: FGFR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093244dup , CM000667.2:g.177093244dup GRCh38
NC_000005.9:g.176520245dup , CM000667.1:g.176520245dup GRCh37
NC_000005.8:g.176452851dup NCBI36
NG_012067.1:g.11325dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1164dup MANE Select ENSP00000292408.4:p.Leu389AlafsTer?
ENST00000292408.8:c.1164dup ENSP00000292408.4:p.Leu389AlafsTer?
ENST00000393637.5:c.1058-88dup ENSP00000377254.1:n.1058-88dup
ENST00000393648.6:c.1097+67dup ENSP00000377259.2:n.1097+67dup
ENST00000502906.5:c.1164dup ENSP00000424960.1:p.Leu389AlafsTer?
ENST00000508139.1:n.468dup
ENST00000511076.1:c.70dup
NM_001291980.1:c.1097+67dup NP_001278909.1:n.1097+67dup
NM_002011.4:c.1164dup NP_002002.3:p.Leu389AlafsTer?
NM_022963.3:c.1058-88dup NP_075252.2:n.1058-88dup
NM_213647.2:c.1164dup NP_998812.1:p.Leu389AlafsTer?
XM_005265838.2:c.1164dup XP_005265895.1:p.Leu389AlafsTer?
XM_011534464.1:c.1257dup XP_011532766.1:p.Leu420AlafsTer?
XM_011534465.1:c.846dup XP_011532767.1:p.Leu283AlafsTer?
XR_941090.1:n.1209dup
NM_001354984.1:c.1164dup NP_001341913.1:p.Leu389AlafsTer?
NM_213647.3:c.1164dup MANE Select NP_998812.1:p.Leu389AlafsTer?
NM_001291980.2:c.1097+67dup NP_001278909.1:n.1097+67dup
NM_001354984.2:c.1164dup NP_001341913.1:p.Leu389AlafsTer?
NM_002011.5:c.1164dup NP_002002.3:p.Leu389AlafsTer?