Canonical Allele Identifier: CA1603393720
Gene: FGFR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177090325T>G , CM000667.2:g.177090325T>G GRCh38
NC_000005.9:g.176517326T>G , CM000667.1:g.176517326T>G GRCh37
NC_000005.8:g.176449932T>G NCBI36
NG_012067.1:g.8406T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.92-65T>G MANE Select ENSP00000292408.4:n.92-65T>G
ENST00000292408.8:c.92-65T>G ENSP00000292408.4:n.92-65T>G
ENST00000393637.5:c.92-65T>G ENSP00000377254.1:n.92-65T>G
ENST00000393648.6:c.92-65T>G ENSP00000377259.2:n.92-65T>G
ENST00000426612.5:n.97-65T>G
ENST00000430285.5:c.175-65T>G ENSP00000395164.1:n.175-65T>G
ENST00000502906.5:c.92-65T>G ENSP00000424960.1:n.92-65T>G
ENST00000503708.5:c.92-65T>G ENSP00000424905.1:n.92-65T>G
ENST00000507708.1:n.248-10T>G
ENST00000509511.5:n.92-65T>G
ENST00000510911.5:c.92-65T>G ENSP00000427222.1:n.92-65T>G
ENST00000513166.1:c.92-65T>G ENSP00000422889.1:n.92-65T>G
ENST00000514472.1:c.92-65T>G ENSP00000426492.1:n.92-65T>G
NM_001291980.1:c.92-65T>G NP_001278909.1:n.92-65T>G
NM_002011.4:c.92-65T>G NP_002002.3:n.92-65T>G
NM_022963.3:c.92-65T>G NP_075252.2:n.92-65T>G
NM_213647.2:c.92-65T>G NP_998812.1:n.92-65T>G
XM_005265838.2:c.92-65T>G XP_005265895.1:n.92-65T>G
XM_011534464.1:c.185-65T>G XP_011532766.1:n.185-65T>G
XM_011534465.1:c.-282-10T>G XP_011532767.1:n.-282-10T>G
XR_941090.1:n.137-65T>G
NM_001354984.1:c.92-65T>G NP_001341913.1:n.92-65T>G
NM_213647.3:c.92-65T>G MANE Select NP_998812.1:n.92-65T>G
NM_001291980.2:c.92-65T>G NP_001278909.1:n.92-65T>G
NM_001354984.2:c.92-65T>G NP_001341913.1:n.92-65T>G
NM_002011.5:c.92-65T>G NP_002002.3:n.92-65T>G