Canonical Allele Identifier: CA362287139

Gene: FGFR4

Linked Data

• ClinVar Variation Id: 2364193
• ClinVar RCV Id: RCV004206370
• dbSNP Id: rs1784352272
• gnomAD v3: 5-177091087-C-T
• gnomAD v4: 5-177091087-C-T
• MyVariant Identifiers: chr5:g.176518088C>T (hg19) ; chr5:g.177091087C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177091087C>T , CM000667.2:g.177091087C>T	GRCh38
NC_000005.9:g.176518088C>T , CM000667.1:g.176518088C>T	GRCh37
NC_000005.8:g.176450694C>T	NCBI36
NG_012067.1:g.9168C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.586C>T MANE Select	ENSP00000292408.4:p.Arg196Cys
ENST00000292408.8:c.586C>T	ENSP00000292408.4:p.Arg196Cys
ENST00000393637.5:c.586C>T	ENSP00000377254.1:p.Arg196Cys
ENST00000393648.6:c.586C>T	ENSP00000377259.2:p.Arg196Cys
ENST00000426612.5:n.703C>T
ENST00000430285.5:c.*450C>T	ENSP00000395164.1:n.*450C>T
ENST00000502906.5:c.586C>T	ENSP00000424960.1:p.Arg196Cys
ENST00000503708.5:c.586C>T	ENSP00000424905.1:p.Arg196Cys
ENST00000509511.5:n.586C>T
NM_001291980.1:c.586C>T	NP_001278909.1:p.Arg196Cys
NM_002011.4:c.586C>T	NP_002002.3:p.Arg196Cys
NM_022963.3:c.586C>T	NP_075252.2:p.Arg196Cys
NM_213647.2:c.586C>T	NP_998812.1:p.Arg196Cys
XM_005265838.2:c.586C>T	XP_005265895.1:p.Arg196Cys
XM_011534464.1:c.679C>T	XP_011532766.1:p.Arg227Cys
XM_011534465.1:c.268C>T	XP_011532767.1:p.Arg90Cys
XR_941090.1:n.631C>T
NM_001354984.1:c.586C>T	NP_001341913.1:p.Arg196Cys
NM_213647.3:c.586C>T MANE Select	NP_998812.1:p.Arg196Cys
NM_001291980.2:c.586C>T	NP_001278909.1:p.Arg196Cys
NM_001354984.2:c.586C>T	NP_001341913.1:p.Arg196Cys
NM_002011.5:c.586C>T	NP_002002.3:p.Arg196Cys