Canonical Allele Identifier: CA1139770270

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093279_177093280insGCCCC , CM000667.2:g.177093279_177093280insGCCCC	GRCh38
NC_000005.9:g.176520280_176520281insGCCCC , CM000667.1:g.176520280_176520281insGCCCC	GRCh37
NC_000005.8:g.176452886_176452887insGCCCC	NCBI36
NG_012067.1:g.11360_11361insGCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1199_1200insGCCCC MANE Select	ENSP00000292408.4:p.Arg401ProfsTer?
ENST00000292408.8:c.1199_1200insGCCCC	ENSP00000292408.4:p.Arg401ProfsTer?
ENST00000393637.5:c.1058-53_1058-52insGCCCC	ENSP00000377254.1:n.1058-53_1058-52insGCCCC
ENST00000393648.6:c.1097+102_1097+103insGCCCC	ENSP00000377259.2:n.1097+102_1097+103insGCCCC
ENST00000502906.5:c.1199_1200insGCCCC	ENSP00000424960.1:p.Arg401ProfsTer?
ENST00000508139.1:n.503_504insGCCCC
ENST00000511076.1:c.105_106insGCCCC
NM_001291980.1:c.1097+102_1097+103insGCCCC	NP_001278909.1:n.1097+102_1097+103insGCCCC
NM_002011.4:c.1199_1200insGCCCC	NP_002002.3:p.Arg401ProfsTer?
NM_022963.3:c.1058-53_1058-52insGCCCC	NP_075252.2:n.1058-53_1058-52insGCCCC
NM_213647.2:c.1199_1200insGCCCC	NP_998812.1:p.Arg401ProfsTer?
XM_005265838.2:c.1199_1200insGCCCC	XP_005265895.1:p.Arg401ProfsTer?
XM_011534464.1:c.1292_1293insGCCCC	XP_011532766.1:p.Arg432ProfsTer?
XM_011534465.1:c.881_882insGCCCC	XP_011532767.1:p.Arg295ProfsTer?
XR_941090.1:n.1244_1245insGCCCC
NM_001354984.1:c.1199_1200insGCCCC	NP_001341913.1:p.Arg401ProfsTer?
NM_213647.3:c.1199_1200insGCCCC MANE Select	NP_998812.1:p.Arg401ProfsTer?
NM_001291980.2:c.1097+102_1097+103insGCCCC	NP_001278909.1:n.1097+102_1097+103insGCCCC
NM_001354984.2:c.1199_1200insGCCCC	NP_001341913.1:p.Arg401ProfsTer?
NM_002011.5:c.1199_1200insGCCCC	NP_002002.3:p.Arg401ProfsTer?