Canonical Allele Identifier: CA362299371

Gene: FGFR4

Linked Data

• COSMIC: COSM5608828 ; COSM5608829
• MyVariant Identifiers: chr5:g.176524345T>C (hg19) ; chr5:g.177097344T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097344T>C , CM000667.2:g.177097344T>C	GRCh38
NC_000005.9:g.176524345T>C , CM000667.1:g.176524345T>C	GRCh37
NC_000005.8:g.176456951T>C	NCBI36
NG_012067.1:g.15425T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.2206T>C MANE Select	ENSP00000292408.4:p.Phe736Leu
ENST00000292408.8:c.2206T>C	ENSP00000292408.4:p.Phe736Leu
ENST00000393637.5:c.2086T>C	ENSP00000377254.1:p.Phe696Leu
ENST00000393648.6:c.2002T>C	ENSP00000377259.2:p.Phe668Leu
ENST00000502906.5:c.2206T>C	ENSP00000424960.1:p.Phe736Leu
ENST00000513423.1:n.154T>C
NM_001291980.1:c.2002T>C	NP_001278909.1:p.Phe668Leu
NM_002011.4:c.2206T>C	NP_002002.3:p.Phe736Leu
NM_022963.3:c.2086T>C	NP_075252.2:p.Phe696Leu
NM_213647.2:c.2206T>C	NP_998812.1:p.Phe736Leu
XM_005265838.2:c.2206T>C	XP_005265895.1:p.Phe736Leu
XM_011534464.1:c.2299T>C	XP_011532766.1:p.Phe767Leu
XM_011534465.1:c.1888T>C	XP_011532767.1:p.Phe630Leu
NM_001354984.1:c.2206T>C	NP_001341913.1:p.Phe736Leu
NM_213647.3:c.2206T>C MANE Select	NP_998812.1:p.Phe736Leu
NM_001291980.2:c.2002T>C	NP_001278909.1:p.Phe668Leu
NM_001354984.2:c.2206T>C	NP_001341913.1:p.Phe736Leu
NM_002011.5:c.2206T>C	NP_002002.3:p.Phe736Leu