Canonical Allele Identifier: CA2711097684

Gene: FGFR4

Linked Data

• dbSNP Id: rs2149731706

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177090948del , CM000667.2:g.177090948del	GRCh38
NC_000005.9:g.176517949del , CM000667.1:g.176517949del	GRCh37
NC_000005.8:g.176450555del	NCBI36
NG_012067.1:g.9029del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.447del MANE Select	ENSP00000292408.4:p.Trp149Ter
ENST00000292408.8:c.447del	ENSP00000292408.4:p.Trp149Ter
ENST00000393637.5:c.447del	ENSP00000377254.1:p.Trp149Ter
ENST00000393648.6:c.447del	ENSP00000377259.2:p.Trp149Ter
ENST00000426612.5:n.564del
ENST00000430285.5:c.*311del	ENSP00000395164.1:n.*311del
ENST00000502906.5:c.447del	ENSP00000424960.1:p.Trp149Ter
ENST00000503708.5:c.447del	ENSP00000424905.1:p.Trp149Ter
ENST00000509511.5:n.447del
NM_001291980.1:c.447del	NP_001278909.1:p.Trp149Ter
NM_002011.4:c.447del	NP_002002.3:p.Trp149Ter
NM_022963.3:c.447del	NP_075252.2:p.Trp149Ter
NM_213647.2:c.447del	NP_998812.1:p.Trp149Ter
XM_005265838.2:c.447del	XP_005265895.1:p.Trp149Ter
XM_011534464.1:c.540del	XP_011532766.1:p.Trp180Ter
XM_011534465.1:c.129del	XP_011532767.1:p.Trp43Ter
XR_941090.1:n.492del
NM_001354984.1:c.447del	NP_001341913.1:p.Trp149Ter
NM_213647.3:c.447del MANE Select	NP_998812.1:p.Trp149Ter
NM_001291980.2:c.447del	NP_001278909.1:p.Trp149Ter
NM_001354984.2:c.447del	NP_001341913.1:p.Trp149Ter
NM_002011.5:c.447del	NP_002002.3:p.Trp149Ter