Canonical Allele Identifier: CA2676682083

Gene: FGFR4

Linked Data

• dbSNP Id: rs2149735394
• gnomAD v4: 5-177093278-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093278_177093279insG , CM000667.2:g.177093278_177093279insG	GRCh38
NC_000005.9:g.176520279_176520280insG , CM000667.1:g.176520279_176520280insG	GRCh37
NC_000005.8:g.176452885_176452886insG	NCBI36
NG_012067.1:g.11359_11360insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1198_1199insG MANE Select	ENSP00000292408.4:p.Pro400ArgfsTer?
ENST00000292408.8:c.1198_1199insG	ENSP00000292408.4:p.Pro400ArgfsTer?
ENST00000393637.5:c.1058-54_1058-53insG	ENSP00000377254.1:n.1058-54_1058-53insG
ENST00000393648.6:c.1097+101_1097+102insG	ENSP00000377259.2:n.1097+101_1097+102insG
ENST00000502906.5:c.1198_1199insG	ENSP00000424960.1:p.Pro400ArgfsTer?
ENST00000508139.1:n.502_503insG
ENST00000511076.1:c.104_105insG
NM_001291980.1:c.1097+101_1097+102insG	NP_001278909.1:n.1097+101_1097+102insG
NM_002011.4:c.1198_1199insG	NP_002002.3:p.Pro400ArgfsTer?
NM_022963.3:c.1058-54_1058-53insG	NP_075252.2:n.1058-54_1058-53insG
NM_213647.2:c.1198_1199insG	NP_998812.1:p.Pro400ArgfsTer?
XM_005265838.2:c.1198_1199insG	XP_005265895.1:p.Pro400ArgfsTer?
XM_011534464.1:c.1291_1292insG	XP_011532766.1:p.Pro431ArgfsTer?
XM_011534465.1:c.880_881insG	XP_011532767.1:p.Pro294ArgfsTer?
XR_941090.1:n.1243_1244insG
NM_001354984.1:c.1198_1199insG	NP_001341913.1:p.Pro400ArgfsTer?
NM_213647.3:c.1198_1199insG MANE Select	NP_998812.1:p.Pro400ArgfsTer?
NM_001291980.2:c.1097+101_1097+102insG	NP_001278909.1:n.1097+101_1097+102insG
NM_001354984.2:c.1198_1199insG	NP_001341913.1:p.Pro400ArgfsTer?
NM_002011.5:c.1198_1199insG	NP_002002.3:p.Pro400ArgfsTer?