Canonical Allele Identifier: CA1603394292

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177090851_177090852delinsTC , CM000667.2:g.177090851_177090852delinsTC	GRCh38
NC_000005.9:g.176517852_176517853delinsTC , CM000667.1:g.176517852_176517853delinsTC	GRCh37
NC_000005.8:g.176450458_176450459delinsTC	NCBI36
NG_012067.1:g.8932_8933delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.436+26_436+27delinsTC MANE Select	ENSP00000292408.4:n.436+26_436+27delinsTC
ENST00000292408.8:c.436+26_436+27delinsTC	ENSP00000292408.4:n.436+26_436+27delinsTC
ENST00000393637.5:c.436+26_436+27delinsTC	ENSP00000377254.1:n.436+26_436+27delinsTC
ENST00000393648.6:c.436+26_436+27delinsTC	ENSP00000377259.2:n.436+26_436+27delinsTC
ENST00000426612.5:n.467_468delinsTC
ENST00000430285.5:c.*300+26_*300+27delinsTC	ENSP00000395164.1:n.*300+26_*300+27delinsTC
ENST00000502906.5:c.436+26_436+27delinsTC	ENSP00000424960.1:n.436+26_436+27delinsTC
ENST00000503708.5:c.436+26_436+27delinsTC	ENSP00000424905.1:n.436+26_436+27delinsTC
ENST00000509511.5:n.436+26_436+27delinsTC
NM_001291980.1:c.436+26_436+27delinsTC	NP_001278909.1:n.436+26_436+27delinsTC
NM_002011.4:c.436+26_436+27delinsTC	NP_002002.3:n.436+26_436+27delinsTC
NM_022963.3:c.436+26_436+27delinsTC	NP_075252.2:n.436+26_436+27delinsTC
NM_213647.2:c.436+26_436+27delinsTC	NP_998812.1:n.436+26_436+27delinsTC
XM_005265838.2:c.436+26_436+27delinsTC	XP_005265895.1:n.436+26_436+27delinsTC
XM_011534464.1:c.529+26_529+27delinsTC	XP_011532766.1:n.529+26_529+27delinsTC
XM_011534465.1:c.118+26_118+27delinsTC	XP_011532767.1:n.118+26_118+27delinsTC
XR_941090.1:n.481+26_481+27delinsTC
NM_001354984.1:c.436+26_436+27delinsTC	NP_001341913.1:n.436+26_436+27delinsTC
NM_213647.3:c.436+26_436+27delinsTC MANE Select	NP_998812.1:n.436+26_436+27delinsTC
NM_001291980.2:c.436+26_436+27delinsTC	NP_001278909.1:n.436+26_436+27delinsTC
NM_001354984.2:c.436+26_436+27delinsTC	NP_001341913.1:n.436+26_436+27delinsTC
NM_002011.5:c.436+26_436+27delinsTC	NP_002002.3:n.436+26_436+27delinsTC