Canonical Allele Identifier: CA447724590

Gene: FGFR4

Linked Data

• COSMIC: COSM48955
• MyVariant Identifiers: chr5:g.176518078del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177091077del , CM000667.2:g.177091077del	GRCh38
NC_000005.9:g.176518078del , CM000667.1:g.176518078del	GRCh37
NC_000005.8:g.176450684del	NCBI36
NG_012067.1:g.9158del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.576del MANE Select	ENSP00000292408.4:p.His192GlnfsTer19
ENST00000292408.8:c.576del	ENSP00000292408.4:p.His192GlnfsTer19
ENST00000393637.5:c.576del	ENSP00000377254.1:p.His192GlnfsTer19
ENST00000393648.6:c.576del	ENSP00000377259.2:p.His192GlnfsTer19
ENST00000426612.5:n.693del
ENST00000430285.5:c.*440del	ENSP00000395164.1:n.*440del
ENST00000502906.5:c.576del	ENSP00000424960.1:p.His192GlnfsTer19
ENST00000503708.5:c.576del	ENSP00000424905.1:p.His192GlnfsTer?
ENST00000509511.5:n.576del
NM_001291980.1:c.576del	NP_001278909.1:p.His192GlnfsTer19
NM_002011.4:c.576del	NP_002002.3:p.His192GlnfsTer19
NM_022963.3:c.576del	NP_075252.2:p.His192GlnfsTer19
NM_213647.2:c.576del	NP_998812.1:p.His192GlnfsTer19
XM_005265838.2:c.576del	XP_005265895.1:p.His192GlnfsTer19
XM_011534464.1:c.669del	XP_011532766.1:p.His223GlnfsTer19
XM_011534465.1:c.258del	XP_011532767.1:p.His86GlnfsTer19
XR_941090.1:n.621del
NM_001354984.1:c.576del	NP_001341913.1:p.His192GlnfsTer19
NM_213647.3:c.576del MANE Select	NP_998812.1:p.His192GlnfsTer19
NM_001291980.2:c.576del	NP_001278909.1:p.His192GlnfsTer19
NM_001354984.2:c.576del	NP_001341913.1:p.His192GlnfsTer19
NM_002011.5:c.576del	NP_002002.3:p.His192GlnfsTer19