Canonical Allele Identifier: CA2676682077

Gene: FGFR4

Linked Data

• dbSNP Id: rs2149735374
• gnomAD v4: 5-177093276-A-ACCG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093278_177093279insGCC , CM000667.2:g.177093278_177093279insGCC	GRCh38
NC_000005.9:g.176520279_176520280insGCC , CM000667.1:g.176520279_176520280insGCC	GRCh37
NC_000005.8:g.176452885_176452886insGCC	NCBI36
NG_012067.1:g.11359_11360insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1198_1199insGCC MANE Select	ENSP00000292408.4:p.His399_Pro400insArg
ENST00000292408.8:c.1198_1199insGCC	ENSP00000292408.4:p.His399_Pro400insArg
ENST00000393637.5:c.1058-54_1058-53insGCC	ENSP00000377254.1:n.1058-54_1058-53insGCC
ENST00000393648.6:c.1097+101_1097+102insGCC	ENSP00000377259.2:n.1097+101_1097+102insGCC
ENST00000502906.5:c.1198_1199insGCC	ENSP00000424960.1:p.His399_Pro400insArg
ENST00000508139.1:n.502_503insGCC
ENST00000511076.1:c.104_105insGCC
NM_001291980.1:c.1097+101_1097+102insGCC	NP_001278909.1:n.1097+101_1097+102insGCC
NM_002011.4:c.1198_1199insGCC	NP_002002.3:p.His399_Pro400insArg
NM_022963.3:c.1058-54_1058-53insGCC	NP_075252.2:n.1058-54_1058-53insGCC
NM_213647.2:c.1198_1199insGCC	NP_998812.1:p.His399_Pro400insArg
XM_005265838.2:c.1198_1199insGCC	XP_005265895.1:p.His399_Pro400insArg
XM_011534464.1:c.1291_1292insGCC	XP_011532766.1:p.His430_Pro431insArg
XM_011534465.1:c.880_881insGCC	XP_011532767.1:p.His293_Pro294insArg
XR_941090.1:n.1243_1244insGCC
NM_001354984.1:c.1198_1199insGCC	NP_001341913.1:p.His399_Pro400insArg
NM_213647.3:c.1198_1199insGCC MANE Select	NP_998812.1:p.His399_Pro400insArg
NM_001291980.2:c.1097+101_1097+102insGCC	NP_001278909.1:n.1097+101_1097+102insGCC
NM_001354984.2:c.1198_1199insGCC	NP_001341913.1:p.His399_Pro400insArg
NM_002011.5:c.1198_1199insGCC	NP_002002.3:p.His399_Pro400insArg