Canonical Allele Identifier: CA362299679

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176524550T>A (hg19) ; chr5:g.177097549T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097549T>A , CM000667.2:g.177097549T>A	GRCh38
NC_000005.9:g.176524550T>A , CM000667.1:g.176524550T>A	GRCh37
NC_000005.8:g.176457156T>A	NCBI36
NG_012067.1:g.15630T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.2282T>A MANE Select	ENSP00000292408.4:p.Phe761Tyr
ENST00000292408.8:c.2282T>A	ENSP00000292408.4:p.Phe761Tyr
ENST00000393637.5:c.2162T>A	ENSP00000377254.1:p.Phe721Tyr
ENST00000393648.6:c.2078T>A	ENSP00000377259.2:p.Phe693Tyr
ENST00000502906.5:c.2282T>A	ENSP00000424960.1:p.Phe761Tyr
ENST00000513423.1:n.230T>A
NM_001291980.1:c.2078T>A	NP_001278909.1:p.Phe693Tyr
NM_002011.4:c.2282T>A	NP_002002.3:p.Phe761Tyr
NM_022963.3:c.2162T>A	NP_075252.2:p.Phe721Tyr
NM_213647.2:c.2282T>A	NP_998812.1:p.Phe761Tyr
XM_005265838.2:c.2282T>A	XP_005265895.1:p.Phe761Tyr
XM_011534464.1:c.2375T>A	XP_011532766.1:p.Phe792Tyr
XM_011534465.1:c.1964T>A	XP_011532767.1:p.Phe655Tyr
NM_001354984.1:c.2282T>A	NP_001341913.1:p.Phe761Tyr
NM_213647.3:c.2282T>A MANE Select	NP_998812.1:p.Phe761Tyr
NM_001291980.2:c.2078T>A	NP_001278909.1:p.Phe693Tyr
NM_001354984.2:c.2282T>A	NP_001341913.1:p.Phe761Tyr
NM_002011.5:c.2282T>A	NP_002002.3:p.Phe761Tyr