Canonical Allele Identifier: CA2984983438

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093256del , CM000667.2:g.177093256del	GRCh38
NC_000005.9:g.176520257del , CM000667.1:g.176520257del	GRCh37
NC_000005.8:g.176452863del	NCBI36
NG_012067.1:g.11337del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1176del MANE Select	ENSP00000292408.4:p.Gln393ArgfsTer?
ENST00000292408.8:c.1176del	ENSP00000292408.4:p.Gln393ArgfsTer?
ENST00000393637.5:c.1058-76del	ENSP00000377254.1:n.1058-76del
ENST00000393648.6:c.1097+79del	ENSP00000377259.2:n.1097+79del
ENST00000502906.5:c.1176del	ENSP00000424960.1:p.Gln393ArgfsTer?
ENST00000508139.1:n.480del
ENST00000511076.1:c.82del
NM_001291980.1:c.1097+79del	NP_001278909.1:n.1097+79del
NM_002011.4:c.1176del	NP_002002.3:p.Gln393ArgfsTer?
NM_022963.3:c.1058-76del	NP_075252.2:n.1058-76del
NM_213647.2:c.1176del	NP_998812.1:p.Gln393ArgfsTer?
XM_005265838.2:c.1176del	XP_005265895.1:p.Gln393ArgfsTer?
XM_011534464.1:c.1269del	XP_011532766.1:p.Gln424ArgfsTer?
XM_011534465.1:c.858del	XP_011532767.1:p.Gln287ArgfsTer?
XR_941090.1:n.1221del
NM_001354984.1:c.1176del	NP_001341913.1:p.Gln393ArgfsTer?
NM_213647.3:c.1176del MANE Select	NP_998812.1:p.Gln393ArgfsTer?
NM_001291980.2:c.1097+79del	NP_001278909.1:n.1097+79del
NM_001354984.2:c.1176del	NP_001341913.1:p.Gln393ArgfsTer?
NM_002011.5:c.1176del	NP_002002.3:p.Gln393ArgfsTer?