Canonical Allele Identifier: CA2676682072

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093276-A-ACCC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093279_177093281dup , CM000667.2:g.177093279_177093281dup	GRCh38
NC_000005.9:g.176520280_176520282dup , CM000667.1:g.176520280_176520282dup	GRCh37
NC_000005.8:g.176452886_176452888dup	NCBI36
NG_012067.1:g.11360_11362dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1199_1201dup MANE Select	ENSP00000292408.4:p.Pro400_Arg401insPro
ENST00000292408.8:c.1199_1201dup	ENSP00000292408.4:p.Pro400_Arg401insPro
ENST00000393637.5:c.1058-53_1058-51dup	ENSP00000377254.1:n.1058-53_1058-51dup
ENST00000393648.6:c.1097+102_1097+104dup	ENSP00000377259.2:n.1097+102_1097+104dup
ENST00000502906.5:c.1199_1201dup	ENSP00000424960.1:p.Pro400_Arg401insPro
ENST00000508139.1:n.503_505dup
ENST00000511076.1:c.105_107dup
NM_001291980.1:c.1097+102_1097+104dup	NP_001278909.1:n.1097+102_1097+104dup
NM_002011.4:c.1199_1201dup	NP_002002.3:p.Pro400_Arg401insPro
NM_022963.3:c.1058-53_1058-51dup	NP_075252.2:n.1058-53_1058-51dup
NM_213647.2:c.1199_1201dup	NP_998812.1:p.Pro400_Arg401insPro
XM_005265838.2:c.1199_1201dup	XP_005265895.1:p.Pro400_Arg401insPro
XM_011534464.1:c.1292_1294dup	XP_011532766.1:p.Pro431_Arg432insPro
XM_011534465.1:c.881_883dup	XP_011532767.1:p.Pro294_Arg295insPro
XR_941090.1:n.1244_1246dup
NM_001354984.1:c.1199_1201dup	NP_001341913.1:p.Pro400_Arg401insPro
NM_213647.3:c.1199_1201dup MANE Select	NP_998812.1:p.Pro400_Arg401insPro
NM_001291980.2:c.1097+102_1097+104dup	NP_001278909.1:n.1097+102_1097+104dup
NM_001354984.2:c.1199_1201dup	NP_001341913.1:p.Pro400_Arg401insPro
NM_002011.5:c.1199_1201dup	NP_002002.3:p.Pro400_Arg401insPro