Canonical Allele Identifier: CA1139771542

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093289_177093290insCCCCCCCCG , CM000667.2:g.177093289_177093290insCCCCCCCCG	GRCh38
NC_000005.9:g.176520290_176520291insCCCCCCCCG , CM000667.1:g.176520290_176520291insCCCCCCCCG	GRCh37
NC_000005.8:g.176452896_176452897insCCCCCCCCG	NCBI36
NG_012067.1:g.11370_11371insCCCCCCCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1209_1210insCCCCCCCCG MANE Select	ENSP00000292408.4:p.Pro403_Ala404insProProPro
ENST00000292408.8:c.1209_1210insCCCCCCCCG	ENSP00000292408.4:p.Pro403_Ala404insProProPro
ENST00000393637.5:c.1058-43_1058-42insCCCCCCCCG	ENSP00000377254.1:n.1058-43_1058-42insCCCCCCCCG
ENST00000393648.6:c.1097+112_1097+113insCCCCCCCCG	ENSP00000377259.2:n.1097+112_1097+113insCCCCCCCCG
ENST00000502906.5:c.1209_1210insCCCCCCCCG	ENSP00000424960.1:p.Pro403_Ala404insProProPro
ENST00000508139.1:n.513_514insCCCCCCCCG
ENST00000511076.1:c.115_116insCCCCCCCCG
NM_001291980.1:c.1097+112_1097+113insCCCCCCCCG	NP_001278909.1:n.1097+112_1097+113insCCCCCCCCG
NM_002011.4:c.1209_1210insCCCCCCCCG	NP_002002.3:p.Pro403_Ala404insProProPro
NM_022963.3:c.1058-43_1058-42insCCCCCCCCG	NP_075252.2:n.1058-43_1058-42insCCCCCCCCG
NM_213647.2:c.1209_1210insCCCCCCCCG	NP_998812.1:p.Pro403_Ala404insProProPro
XM_005265838.2:c.1209_1210insCCCCCCCCG	XP_005265895.1:p.Pro403_Ala404insProProPro
XM_011534464.1:c.1302_1303insCCCCCCCCG	XP_011532766.1:p.Pro434_Ala435insProProPro
XM_011534465.1:c.891_892insCCCCCCCCG	XP_011532767.1:p.Pro297_Ala298insProProPro
XR_941090.1:n.1254_1255insCCCCCCCCG
NM_001354984.1:c.1209_1210insCCCCCCCCG	NP_001341913.1:p.Pro403_Ala404insProProPro
NM_213647.3:c.1209_1210insCCCCCCCCG MANE Select	NP_998812.1:p.Pro403_Ala404insProProPro
NM_001291980.2:c.1097+112_1097+113insCCCCCCCCG	NP_001278909.1:n.1097+112_1097+113insCCCCCCCCG
NM_001354984.2:c.1209_1210insCCCCCCCCG	NP_001341913.1:p.Pro403_Ala404insProProPro
NM_002011.5:c.1209_1210insCCCCCCCCG	NP_002002.3:p.Pro403_Ala404insProProPro