Canonical Allele Identifier: CA2984983428

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093148dup , CM000667.2:g.177093148dup	GRCh38
NC_000005.9:g.176520149dup , CM000667.1:g.176520149dup	GRCh37
NC_000005.8:g.176452755dup	NCBI36
NG_012067.1:g.11229dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1068dup MANE Select	ENSP00000292408.4:p.Thr357HisfsTer?
ENST00000292408.8:c.1068dup	ENSP00000292408.4:p.Thr357HisfsTer?
ENST00000393637.5:c.1058-184dup	ENSP00000377254.1:n.1058-184dup
ENST00000393648.6:c.1068dup	ENSP00000377259.2:p.Thr357HisfsTer?
ENST00000502906.5:c.1068dup	ENSP00000424960.1:p.Thr357HisfsTer?
ENST00000508139.1:n.372dup
NM_001291980.1:c.1068dup	NP_001278909.1:p.Thr357HisfsTer?
NM_002011.4:c.1068dup	NP_002002.3:p.Thr357HisfsTer?
NM_022963.3:c.1058-184dup	NP_075252.2:n.1058-184dup
NM_213647.2:c.1068dup	NP_998812.1:p.Thr357HisfsTer?
XM_005265838.2:c.1068dup	XP_005265895.1:p.Thr357HisfsTer?
XM_011534464.1:c.1161dup	XP_011532766.1:p.Thr388HisfsTer?
XM_011534465.1:c.750dup	XP_011532767.1:p.Thr251HisfsTer?
XR_941090.1:n.1113dup
NM_001354984.1:c.1068dup	NP_001341913.1:p.Thr357HisfsTer?
NM_213647.3:c.1068dup MANE Select	NP_998812.1:p.Thr357HisfsTer?
NM_001291980.2:c.1068dup	NP_001278909.1:p.Thr357HisfsTer?
NM_001354984.2:c.1068dup	NP_001341913.1:p.Thr357HisfsTer?
NM_002011.5:c.1068dup	NP_002002.3:p.Thr357HisfsTer?