Canonical Allele Identifier: CA2711101616

Gene: FGFR4

Linked Data

• dbSNP Id: rs2149735527

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093320del , CM000667.2:g.177093320del	GRCh38
NC_000005.9:g.176520321del , CM000667.1:g.176520321del	GRCh37
NC_000005.8:g.176452927del	NCBI36
NG_012067.1:g.11401del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1240del MANE Select	ENSP00000292408.4:p.Leu414TrpfsTer?
ENST00000292408.8:c.1240del	ENSP00000292408.4:p.Leu414TrpfsTer?
ENST00000393637.5:c.1058-12del	ENSP00000377254.1:n.1058-12del
ENST00000393648.6:c.1098-86del	ENSP00000377259.2:n.1098-86del
ENST00000502906.5:c.1240del	ENSP00000424960.1:p.Leu414TrpfsTer?
ENST00000508139.1:n.544del
ENST00000511076.1:c.146del
NM_001291980.1:c.1098-86del	NP_001278909.1:n.1098-86del
NM_002011.4:c.1240del	NP_002002.3:p.Leu414TrpfsTer?
NM_022963.3:c.1058-12del	NP_075252.2:n.1058-12del
NM_213647.2:c.1240del	NP_998812.1:p.Leu414TrpfsTer?
XM_005265838.2:c.1240del	XP_005265895.1:p.Leu414TrpfsTer?
XM_011534464.1:c.1333del	XP_011532766.1:p.Leu445TrpfsTer?
XM_011534465.1:c.922del	XP_011532767.1:p.Leu308TrpfsTer?
XR_941090.1:n.1285del
NM_001354984.1:c.1240del	NP_001341913.1:p.Leu414TrpfsTer?
NM_213647.3:c.1240del MANE Select	NP_998812.1:p.Leu414TrpfsTer?
NM_001291980.2:c.1098-86del	NP_001278909.1:n.1098-86del
NM_001354984.2:c.1240del	NP_001341913.1:p.Leu414TrpfsTer?
NM_002011.5:c.1240del	NP_002002.3:p.Leu414TrpfsTer?