Canonical Allele Identifier: CA1603396976

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093258_177093261delinsAGGC , CM000667.2:g.177093258_177093261delinsAGGC	GRCh38
NC_000005.9:g.176520259_176520262delinsAGGC , CM000667.1:g.176520259_176520262delinsAGGC	GRCh37
NC_000005.8:g.176452865_176452868delinsAGGC	NCBI36
NG_012067.1:g.11339_11342delinsAGGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.1178_1181delinsAGGC MANE Select	ENSP00000292408.4:p.Gln393=
ENST00000292408.8:c.1178_1181delinsAGGC	ENSP00000292408.4:p.Gln393=
ENST00000393637.5:c.1058-74_1058-71delinsAGGC	ENSP00000377254.1:n.1058-74_1058-71delins...
ENST00000393648.6:c.1097+81_1097+84delinsAGGC	ENSP00000377259.2:n.1097+81_1097+84delins...
ENST00000502906.5:c.1178_1181delinsAGGC	ENSP00000424960.1:p.Gln393=
ENST00000508139.1:n.482_485delinsAGGC
ENST00000511076.1:c.84_87delinsAGGC
NM_001291980.1:c.1097+81_1097+84delinsAGGC	NP_001278909.1:n.1097+81_1097+84delinsAGG...
NM_002011.4:c.1178_1181delinsAGGC	NP_002002.3:p.Gln393=
NM_022963.3:c.1058-74_1058-71delinsAGGC	NP_075252.2:n.1058-74_1058-71delinsAGGC
NM_213647.2:c.1178_1181delinsAGGC	NP_998812.1:p.Gln393=
XM_005265838.2:c.1178_1181delinsAGGC	XP_005265895.1:p.Gln393=
XM_011534464.1:c.1271_1274delinsAGGC	XP_011532766.1:p.Gln424=
XM_011534465.1:c.860_863delinsAGGC	XP_011532767.1:p.Gln287=
XR_941090.1:n.1223_1226delinsAGGC
NM_001354984.1:c.1178_1181delinsAGGC	NP_001341913.1:p.Gln393=
NM_213647.3:c.1178_1181delinsAGGC MANE Select	NP_998812.1:p.Gln393=
NM_001291980.2:c.1097+81_1097+84delinsAGGC	NP_001278909.1:n.1097+81_1097+84delinsAGG...
NM_001354984.2:c.1178_1181delinsAGGC	NP_001341913.1:p.Gln393=
NM_002011.5:c.1178_1181delinsAGGC	NP_002002.3:p.Gln393=