Canonical Allele Identifier: CA362289599

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176519676G>C (hg19) ; chr5:g.177092675G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177092675G>C , CM000667.2:g.177092675G>C	GRCh38
NC_000005.9:g.176519676G>C , CM000667.1:g.176519676G>C	GRCh37
NC_000005.8:g.176452282G>C	NCBI36
NG_012067.1:g.10756G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.948G>C MANE Select	ENSP00000292408.4:p.Glu316Asp
ENST00000292408.8:c.948G>C	ENSP00000292408.4:p.Glu316Asp
ENST00000393637.5:c.948G>C	ENSP00000377254.1:p.Glu316Asp
ENST00000393648.6:c.948G>C	ENSP00000377259.2:p.Glu316Asp
ENST00000502906.5:c.948G>C	ENSP00000424960.1:p.Glu316Asp
ENST00000508139.1:n.252G>C
ENST00000509511.5:n.948G>C
NM_001291980.1:c.948G>C	NP_001278909.1:p.Glu316Asp
NM_002011.4:c.948G>C	NP_002002.3:p.Glu316Asp
NM_022963.3:c.948G>C	NP_075252.2:p.Glu316Asp
NM_213647.2:c.948G>C	NP_998812.1:p.Glu316Asp
XM_005265838.2:c.948G>C	XP_005265895.1:p.Glu316Asp
XM_011534464.1:c.1041G>C	XP_011532766.1:p.Glu347Asp
XM_011534465.1:c.630G>C	XP_011532767.1:p.Glu210Asp
XR_941090.1:n.993G>C
NM_001354984.1:c.948G>C	NP_001341913.1:p.Glu316Asp
NM_213647.3:c.948G>C MANE Select	NP_998812.1:p.Glu316Asp
NM_001291980.2:c.948G>C	NP_001278909.1:p.Glu316Asp
NM_001354984.2:c.948G>C	NP_001341913.1:p.Glu316Asp
NM_002011.5:c.948G>C	NP_002002.3:p.Glu316Asp