Canonical Allele Identifier: CA2676681584

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177092602-G-GCCCCAGGCCCTGCTGTGA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177092609_177092626dup , CM000667.2:g.177092609_177092626dup	GRCh38
NC_000005.9:g.176519610_176519627dup , CM000667.1:g.176519610_176519627dup	GRCh37
NC_000005.8:g.176452216_176452233dup	NCBI36
NG_012067.1:g.10690_10707dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.919-37_919-20dup MANE Select	ENSP00000292408.4:n.919-37_919-20dup
ENST00000292408.8:c.919-37_919-20dup	ENSP00000292408.4:n.919-37_919-20dup
ENST00000393637.5:c.919-37_919-20dup	ENSP00000377254.1:n.919-37_919-20dup
ENST00000393648.6:c.919-37_919-20dup	ENSP00000377259.2:n.919-37_919-20dup
ENST00000502906.5:c.919-37_919-20dup	ENSP00000424960.1:n.919-37_919-20dup
ENST00000508139.1:n.223-37_223-20dup
ENST00000509511.5:n.919-37_919-20dup
NM_001291980.1:c.919-37_919-20dup	NP_001278909.1:n.919-37_919-20dup
NM_002011.4:c.919-37_919-20dup	NP_002002.3:n.919-37_919-20dup
NM_022963.3:c.919-37_919-20dup	NP_075252.2:n.919-37_919-20dup
NM_213647.2:c.919-37_919-20dup	NP_998812.1:n.919-37_919-20dup
XM_005265838.2:c.919-37_919-20dup	XP_005265895.1:n.919-37_919-20dup
XM_011534464.1:c.1012-37_1012-20dup	XP_011532766.1:n.1012-37_1012-20dup
XM_011534465.1:c.601-37_601-20dup	XP_011532767.1:n.601-37_601-20dup
XR_941090.1:n.964-37_964-20dup
NM_001354984.1:c.919-37_919-20dup	NP_001341913.1:n.919-37_919-20dup
NM_213647.3:c.919-37_919-20dup MANE Select	NP_998812.1:n.919-37_919-20dup
NM_001291980.2:c.919-37_919-20dup	NP_001278909.1:n.919-37_919-20dup
NM_001354984.2:c.919-37_919-20dup	NP_001341913.1:n.919-37_919-20dup
NM_002011.5:c.919-37_919-20dup	NP_002002.3:n.919-37_919-20dup