Canonical Allele Identifier: CA1603397035

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093278_177093282delinsCCCCG , CM000667.2:g.177093278_177093282delinsCCCCG	GRCh38
NC_000005.9:g.176520279_176520283delinsCCCCG , CM000667.1:g.176520279_176520283delinsCCCCG	GRCh37
NC_000005.8:g.176452885_176452889delinsCCCCG	NCBI36
NG_012067.1:g.11359_11363delinsCCCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1198_1202delinsCCCCG MANE Select	ENSP00000292408.4:p.Pro400=
ENST00000292408.8:c.1198_1202delinsCCCCG	ENSP00000292408.4:p.Pro400=
ENST00000393637.5:c.1058-54_1058-50delinsCCCCG	ENSP00000377254.1:n.1058-54_1058-50delinsCCCCG
ENST00000393648.6:c.1097+101_1097+105delinsCCCCG	ENSP00000377259.2:n.1097+101_1097+105delinsCCCCG
ENST00000502906.5:c.1198_1202delinsCCCCG	ENSP00000424960.1:p.Pro400=
ENST00000508139.1:n.502_506delinsCCCCG
ENST00000511076.1:c.104_108delinsCCCCG
NM_001291980.1:c.1097+101_1097+105delinsCCCCG	NP_001278909.1:n.1097+101_1097+105delinsCCCCG
NM_002011.4:c.1198_1202delinsCCCCG	NP_002002.3:p.Pro400=
NM_022963.3:c.1058-54_1058-50delinsCCCCG	NP_075252.2:n.1058-54_1058-50delinsCCCCG
NM_213647.2:c.1198_1202delinsCCCCG	NP_998812.1:p.Pro400=
XM_005265838.2:c.1198_1202delinsCCCCG	XP_005265895.1:p.Pro400=
XM_011534464.1:c.1291_1295delinsCCCCG	XP_011532766.1:p.Pro431=
XM_011534465.1:c.880_884delinsCCCCG	XP_011532767.1:p.Pro294=
XR_941090.1:n.1243_1247delinsCCCCG
NM_001354984.1:c.1198_1202delinsCCCCG	NP_001341913.1:p.Pro400=
NM_213647.3:c.1198_1202delinsCCCCG MANE Select	NP_998812.1:p.Pro400=
NM_001291980.2:c.1097+101_1097+105delinsCCCCG	NP_001278909.1:n.1097+101_1097+105delinsCCCCG
NM_001354984.2:c.1198_1202delinsCCCCG	NP_001341913.1:p.Pro400=
NM_002011.5:c.1198_1202delinsCCCCG	NP_002002.3:p.Pro400=