Canonical Allele Identifier: CA1603396831

Gene: FGFR4

Linked Data

• dbSNP Id: rs1784428091
• gnomAD v4: 5-177093174-C-CCAGGTATACGGACAT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093177_177093191dup , CM000667.2:g.177093177_177093191dup	GRCh38
NC_000005.9:g.176520178_176520192dup , CM000667.1:g.176520178_176520192dup	GRCh37
NC_000005.8:g.176452784_176452798dup	NCBI36
NG_012067.1:g.11258_11272dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1097_1111dup MANE Select	ENSP00000292408.4:p.Ile370_Ile371insArgTyrThrAspIle
ENST00000292408.8:c.1097_1111dup	ENSP00000292408.4:p.Ile370_Ile371insArgTyrThrAspIle
ENST00000393637.5:c.1058-155_1058-141dup	ENSP00000377254.1:n.1058-155_1058-141dup
ENST00000393648.6:c.1097_1097+14dup
ENST00000502906.5:c.1097_1111dup	ENSP00000424960.1:p.Ile370_Ile371insArgTyrThrAspIle
ENST00000508139.1:n.401_415dup
ENST00000511076.1:c.3_17dup
NM_001291980.1:c.1097_1097+14dup
NM_002011.4:c.1097_1111dup	NP_002002.3:p.Ile370_Ile371insArgTyrThrAspIle
NM_022963.3:c.1058-155_1058-141dup	NP_075252.2:n.1058-155_1058-141dup
NM_213647.2:c.1097_1111dup	NP_998812.1:p.Ile370_Ile371insArgTyrThrAspIle
XM_005265838.2:c.1097_1111dup	XP_005265895.1:p.Ile370_Ile371insArgTyrThrAspIle
XM_011534464.1:c.1190_1204dup	XP_011532766.1:p.Ile401_Ile402insArgTyrThrAspIle
XM_011534465.1:c.779_793dup	XP_011532767.1:p.Ile264_Ile265insArgTyrThrAspIle
XR_941090.1:n.1142_1156dup
NM_001354984.1:c.1097_1111dup	NP_001341913.1:p.Ile370_Ile371insArgTyrThrAspIle
NM_213647.3:c.1097_1111dup MANE Select	NP_998812.1:p.Ile370_Ile371insArgTyrThrAspIle
NM_001291980.2:c.1097_1097+14dup
NM_001354984.2:c.1097_1111dup	NP_001341913.1:p.Ile370_Ile371insArgTyrThrAspIle
NM_002011.5:c.1097_1111dup	NP_002002.3:p.Ile370_Ile371insArgTyrThrAspIle