Canonical Allele Identifier: CA2676681074
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177091155_177091156dup , CM000667.2:g.177091155_177091156dup GRCh38
NC_000005.9:g.176518156_176518157dup , CM000667.1:g.176518156_176518157dup GRCh37
NC_000005.8:g.176450762_176450763dup NCBI36
NG_012067.1:g.9236_9237dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.603+51_603+52dup MANE Select ENSP00000292408.4:n.603+51_603+52dup
ENST00000292408.8:c.603+51_603+52dup ENSP00000292408.4:n.603+51_603+52dup
ENST00000393637.5:c.603+51_603+52dup ENSP00000377254.1:n.603+51_603+52dup
ENST00000393648.6:c.603+51_603+52dup ENSP00000377259.2:n.603+51_603+52dup
ENST00000502906.5:c.603+51_603+52dup ENSP00000424960.1:n.603+51_603+52dup
ENST00000509511.5:n.603+51_603+52dup
NM_001291980.1:c.603+51_603+52dup NP_001278909.1:n.603+51_603+52dup
NM_002011.4:c.603+51_603+52dup NP_002002.3:n.603+51_603+52dup
NM_022963.3:c.603+51_603+52dup NP_075252.2:n.603+51_603+52dup
NM_213647.2:c.603+51_603+52dup NP_998812.1:n.603+51_603+52dup
XM_005265838.2:c.603+51_603+52dup XP_005265895.1:n.603+51_603+52dup
XM_011534464.1:c.696+51_696+52dup XP_011532766.1:n.696+51_696+52dup
XM_011534465.1:c.285+51_285+52dup XP_011532767.1:n.285+51_285+52dup
XR_941090.1:n.648+51_648+52dup
NM_001354984.1:c.603+51_603+52dup NP_001341913.1:n.603+51_603+52dup
NM_213647.3:c.603+51_603+52dup MANE Select NP_998812.1:n.603+51_603+52dup
NM_001291980.2:c.603+51_603+52dup NP_001278909.1:n.603+51_603+52dup
NM_001354984.2:c.603+51_603+52dup NP_001341913.1:n.603+51_603+52dup
NM_002011.5:c.603+51_603+52dup NP_002002.3:n.603+51_603+52dup