Canonical Allele Identifier: CA362287010

Gene: FGFR4

Linked Data

• COSMIC: COSM4141698 ; COSM4141699
• MyVariant Identifiers: chr5:g.176518028G>T (hg19) ; chr5:g.177091027G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177091027G>T , CM000667.2:g.177091027G>T	GRCh38
NC_000005.9:g.176518028G>T , CM000667.1:g.176518028G>T	GRCh37
NC_000005.8:g.176450634G>T	NCBI36
NG_012067.1:g.9108G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.526G>T MANE Select	ENSP00000292408.4:p.Gly176Cys
ENST00000292408.8:c.526G>T	ENSP00000292408.4:p.Gly176Cys
ENST00000393637.5:c.526G>T	ENSP00000377254.1:p.Gly176Cys
ENST00000393648.6:c.526G>T	ENSP00000377259.2:p.Gly176Cys
ENST00000426612.5:n.643G>T
ENST00000430285.5:c.*390G>T	ENSP00000395164.1:n.*390G>T
ENST00000502906.5:c.526G>T	ENSP00000424960.1:p.Gly176Cys
ENST00000503708.5:c.526G>T	ENSP00000424905.1:p.Gly176Cys
ENST00000509511.5:n.526G>T
NM_001291980.1:c.526G>T	NP_001278909.1:p.Gly176Cys
NM_002011.4:c.526G>T	NP_002002.3:p.Gly176Cys
NM_022963.3:c.526G>T	NP_075252.2:p.Gly176Cys
NM_213647.2:c.526G>T	NP_998812.1:p.Gly176Cys
XM_005265838.2:c.526G>T	XP_005265895.1:p.Gly176Cys
XM_011534464.1:c.619G>T	XP_011532766.1:p.Gly207Cys
XM_011534465.1:c.208G>T	XP_011532767.1:p.Gly70Cys
XR_941090.1:n.571G>T
NM_001354984.1:c.526G>T	NP_001341913.1:p.Gly176Cys
NM_213647.3:c.526G>T MANE Select	NP_998812.1:p.Gly176Cys
NM_001291980.2:c.526G>T	NP_001278909.1:p.Gly176Cys
NM_001354984.2:c.526G>T	NP_001341913.1:p.Gly176Cys
NM_002011.5:c.526G>T	NP_002002.3:p.Gly176Cys