Canonical Allele Identifier: CA2711096186

Gene: FGFR4

Linked Data

• dbSNP Id: rs2149731207

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177090696_177090700del , CM000667.2:g.177090696_177090700del	GRCh38
NC_000005.9:g.176517697_176517701del , CM000667.1:g.176517697_176517701del	GRCh37
NC_000005.8:g.176450303_176450307del	NCBI36
NG_012067.1:g.8777_8781del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.355+43_356-45del MANE Select	ENSP00000292408.4:n.355+43_356-45del
ENST00000292408.8:c.355+43_356-45del	ENSP00000292408.4:n.355+43_356-45del
ENST00000393637.5:c.355+43_356-45del	ENSP00000377254.1:n.355+43_356-45del
ENST00000393648.6:c.355+43_356-45del	ENSP00000377259.2:n.355+43_356-45del
ENST00000426612.5:n.360+43_361-45del
ENST00000430285.5:c.*219+43_*220-45del	ENSP00000395164.1:n.*219+43_*220-45del
ENST00000502906.5:c.355+43_356-45del	ENSP00000424960.1:n.355+43_356-45del
ENST00000503708.5:c.355+43_356-45del	ENSP00000424905.1:n.355+43_356-45del
ENST00000509511.5:n.355+43_356-45del
NM_001291980.1:c.355+43_356-45del	NP_001278909.1:n.355+43_356-45del
NM_002011.4:c.355+43_356-45del	NP_002002.3:n.355+43_356-45del
NM_022963.3:c.355+43_356-45del	NP_075252.2:n.355+43_356-45del
NM_213647.2:c.355+43_356-45del	NP_998812.1:n.355+43_356-45del
XM_005265838.2:c.355+43_356-45del	XP_005265895.1:n.355+43_356-45del
XM_011534464.1:c.448+43_449-45del	XP_011532766.1:n.448+43_449-45del
XM_011534465.1:c.37+43_38-45del	XP_011532767.1:n.37+43_38-45del
XR_941090.1:n.400+43_401-45del
NM_001354984.1:c.355+43_356-45del	NP_001341913.1:n.355+43_356-45del
NM_213647.3:c.355+43_356-45del MANE Select	NP_998812.1:n.355+43_356-45del
NM_001291980.2:c.355+43_356-45del	NP_001278909.1:n.355+43_356-45del
NM_001354984.2:c.355+43_356-45del	NP_001341913.1:n.355+43_356-45del
NM_002011.5:c.355+43_356-45del	NP_002002.3:n.355+43_356-45del