Canonical Allele Identifier: CA3038604312

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093248_177093251del , CM000667.2:g.177093248_177093251del	GRCh38
NC_000005.9:g.176520249_176520252del , CM000667.1:g.176520249_176520252del	GRCh37
NC_000005.8:g.176452855_176452858del	NCBI36
NG_012067.1:g.11329_11332del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1168_1171del MANE Select	ENSP00000292408.4:p.Tyr390GlufsTer?
ENST00000292408.8:c.1168_1171del	ENSP00000292408.4:p.Tyr390GlufsTer?
ENST00000393637.5:c.1058-84_1058-81del	ENSP00000377254.1:n.1058-84_1058-81del
ENST00000393648.6:c.1097+71_1097+74del	ENSP00000377259.2:n.1097+71_1097+74del
ENST00000502906.5:c.1168_1171del	ENSP00000424960.1:p.Tyr390GlufsTer?
ENST00000508139.1:n.472_475del
ENST00000511076.1:c.74_77del
NM_001291980.1:c.1097+71_1097+74del	NP_001278909.1:n.1097+71_1097+74del
NM_002011.4:c.1168_1171del	NP_002002.3:p.Tyr390GlufsTer?
NM_022963.3:c.1058-84_1058-81del	NP_075252.2:n.1058-84_1058-81del
NM_213647.2:c.1168_1171del	NP_998812.1:p.Tyr390GlufsTer?
XM_005265838.2:c.1168_1171del	XP_005265895.1:p.Tyr390GlufsTer?
XM_011534464.1:c.1261_1264del	XP_011532766.1:p.Tyr421GlufsTer?
XM_011534465.1:c.850_853del	XP_011532767.1:p.Tyr284GlufsTer?
XR_941090.1:n.1213_1216del
NM_001354984.1:c.1168_1171del	NP_001341913.1:p.Tyr390GlufsTer?
NM_213647.3:c.1168_1171del MANE Select	NP_998812.1:p.Tyr390GlufsTer?
NM_001291980.2:c.1097+71_1097+74del	NP_001278909.1:n.1097+71_1097+74del
NM_001354984.2:c.1168_1171del	NP_001341913.1:p.Tyr390GlufsTer?
NM_002011.5:c.1168_1171del	NP_002002.3:p.Tyr390GlufsTer?