Canonical Allele Identifier: CA1139770269

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093276-A-ACCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093281_177093282insCCCCCC , CM000667.2:g.177093281_177093282insCCCCCC	GRCh38
NC_000005.9:g.176520282_176520283insCCCCCC , CM000667.1:g.176520282_176520283insCCCCCC	GRCh37
NC_000005.8:g.176452888_176452889insCCCCCC	NCBI36
NG_012067.1:g.11362_11363insCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1201_1202insCCCCCC MANE Select	ENSP00000292408.4:p.Pro400_Arg401insProPro
ENST00000292408.8:c.1201_1202insCCCCCC	ENSP00000292408.4:p.Pro400_Arg401insProPro
ENST00000393637.5:c.1058-51_1058-50insCCCCCC	ENSP00000377254.1:n.1058-51_1058-50insCCCCCC
ENST00000393648.6:c.1097+104_1097+105insCCCCCC	ENSP00000377259.2:n.1097+104_1097+105insCCCCCC
ENST00000502906.5:c.1201_1202insCCCCCC	ENSP00000424960.1:p.Pro400_Arg401insProPro
ENST00000508139.1:n.505_506insCCCCCC
ENST00000511076.1:c.107_108insCCCCCC
NM_001291980.1:c.1097+104_1097+105insCCCCCC	NP_001278909.1:n.1097+104_1097+105insCCCCCC
NM_002011.4:c.1201_1202insCCCCCC	NP_002002.3:p.Pro400_Arg401insProPro
NM_022963.3:c.1058-51_1058-50insCCCCCC	NP_075252.2:n.1058-51_1058-50insCCCCCC
NM_213647.2:c.1201_1202insCCCCCC	NP_998812.1:p.Pro400_Arg401insProPro
XM_005265838.2:c.1201_1202insCCCCCC	XP_005265895.1:p.Pro400_Arg401insProPro
XM_011534464.1:c.1294_1295insCCCCCC	XP_011532766.1:p.Pro431_Arg432insProPro
XM_011534465.1:c.883_884insCCCCCC	XP_011532767.1:p.Pro294_Arg295insProPro
XR_941090.1:n.1246_1247insCCCCCC
NM_001354984.1:c.1201_1202insCCCCCC	NP_001341913.1:p.Pro400_Arg401insProPro
NM_213647.3:c.1201_1202insCCCCCC MANE Select	NP_998812.1:p.Pro400_Arg401insProPro
NM_001291980.2:c.1097+104_1097+105insCCCCCC	NP_001278909.1:n.1097+104_1097+105insCCCCCC
NM_001354984.2:c.1201_1202insCCCCCC	NP_001341913.1:p.Pro400_Arg401insProPro
NM_002011.5:c.1201_1202insCCCCCC	NP_002002.3:p.Pro400_Arg401insProPro