Canonical Allele Identifier: CA362291437
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093243G>T , CM000667.2:g.177093243G>T GRCh38
NC_000005.9:g.176520244G>T , CM000667.1:g.176520244G>T GRCh37
NC_000005.8:g.176452850G>T NCBI36
NG_012067.1:g.11324G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000292408.9:c.1163G>T MANE Select ENSP00000292408.4:p.Gly388Val
ENST00000292408.8:c.1163G>T ENSP00000292408.4:p.Gly388Val
ENST00000393637.5:c.1058-89G>T ENSP00000377254.1:n.1058-89G>T
ENST00000393648.6:c.1097+66G>T ENSP00000377259.2:n.1097+66G>T
ENST00000502906.5:c.1163G>T ENSP00000424960.1:p.Gly388Val
ENST00000508139.1:n.467G>T
ENST00000511076.1:c.69G>T
NM_001291980.1:c.1097+66G>T NP_001278909.1:n.1097+66G>T
NM_002011.4:c.1163G>T NP_002002.3:p.Gly388Val
NM_022963.3:c.1058-89G>T NP_075252.2:n.1058-89G>T
NM_213647.2:c.1163G>T NP_998812.1:p.Gly388Val
XM_005265838.2:c.1163G>T XP_005265895.1:p.Gly388Val
XM_011534464.1:c.1256G>T XP_011532766.1:p.Gly419Val
XM_011534465.1:c.845G>T XP_011532767.1:p.Gly282Val
XR_941090.1:n.1208G>T
NM_001354984.1:c.1163G>T NP_001341913.1:p.Gly388Val
NM_213647.3:c.1163G>T MANE Select NP_998812.1:p.Gly388Val
NM_001291980.2:c.1097+66G>T NP_001278909.1:n.1097+66G>T
NM_001354984.2:c.1163G>T NP_001341913.1:p.Gly388Val
NM_002011.5:c.1163G>T NP_002002.3:p.Gly388Val