Canonical Allele Identifier: CA2676682294

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093526-C-CCACTATGG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093527_177093534dup , CM000667.2:g.177093527_177093534dup	GRCh38
NC_000005.9:g.176520528_176520535dup , CM000667.1:g.176520528_176520535dup	GRCh37
NC_000005.8:g.176453134_176453141dup	NCBI36
NG_012067.1:g.11608_11615dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1373_1380dup MANE Select	ENSP00000292408.4:p.Glu461HisfsTer16
ENST00000292408.8:c.1373_1380dup	ENSP00000292408.4:p.Glu461HisfsTer16
ENST00000393637.5:c.1253_1260dup	ENSP00000377254.1:p.Glu421HisfsTer16
ENST00000393648.6:c.1193+26_1193+33dup	ENSP00000377259.2:n.1193+26_1193+33dup
ENST00000502906.5:c.1373_1380dup	ENSP00000424960.1:p.Glu461HisfsTer16
ENST00000511076.1:c.267_274dup
NM_001291980.1:c.1193+26_1193+33dup	NP_001278909.1:n.1193+26_1193+33dup
NM_002011.4:c.1373_1380dup	NP_002002.3:p.Glu461HisfsTer16
NM_022963.3:c.1253_1260dup	NP_075252.2:p.Glu421HisfsTer16
NM_213647.2:c.1373_1380dup	NP_998812.1:p.Glu461HisfsTer16
XM_005265838.2:c.1373_1380dup	XP_005265895.1:p.Glu461HisfsTer16
XM_011534464.1:c.1466_1473dup	XP_011532766.1:p.Glu492HisfsTer16
XM_011534465.1:c.1055_1062dup	XP_011532767.1:p.Glu355HisfsTer16
XR_941090.1:n.1392+26_1392+33dup
NM_001354984.1:c.1373_1380dup	NP_001341913.1:p.Glu461HisfsTer16
NM_213647.3:c.1373_1380dup MANE Select	NP_998812.1:p.Glu461HisfsTer16
NM_001291980.2:c.1193+26_1193+33dup	NP_001278909.1:n.1193+26_1193+33dup
NM_001354984.2:c.1373_1380dup	NP_001341913.1:p.Glu461HisfsTer16
NM_002011.5:c.1373_1380dup	NP_002002.3:p.Glu461HisfsTer16