Canonical Allele Identifier: CA362286662

Gene: FGFR4

Linked Data

• dbSNP Id: rs376618
• MyVariant Identifiers: chr5:g.176517797C>G (hg19) ; chr5:g.177090796C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177090796C>G , CM000667.2:g.177090796C>G	GRCh38
NC_000005.9:g.176517797C>G , CM000667.1:g.176517797C>G	GRCh37
NC_000005.8:g.176450403C>G	NCBI36
NG_012067.1:g.8877C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.407C>G MANE Select	ENSP00000292408.4:p.Pro136Arg
ENST00000292408.8:c.407C>G	ENSP00000292408.4:p.Pro136Arg
ENST00000393637.5:c.407C>G	ENSP00000377254.1:p.Pro136Arg
ENST00000393648.6:c.407C>G	ENSP00000377259.2:p.Pro136Arg
ENST00000426612.5:n.412C>G
ENST00000430285.5:c.*271C>G	ENSP00000395164.1:n.*271C>G
ENST00000502906.5:c.407C>G	ENSP00000424960.1:p.Pro136Arg
ENST00000503708.5:c.407C>G	ENSP00000424905.1:p.Pro136Arg
ENST00000509511.5:n.407C>G
NM_001291980.1:c.407C>G	NP_001278909.1:p.Pro136Arg
NM_002011.4:c.407C>G	NP_002002.3:p.Pro136Arg
NM_022963.3:c.407C>G	NP_075252.2:p.Pro136Arg
NM_213647.2:c.407C>G	NP_998812.1:p.Pro136Arg
XM_005265838.2:c.407C>G	XP_005265895.1:p.Pro136Arg
XM_011534464.1:c.500C>G	XP_011532766.1:p.Pro167Arg
XM_011534465.1:c.89C>G	XP_011532767.1:p.Pro30Arg
XR_941090.1:n.452C>G
NM_001354984.1:c.407C>G	NP_001341913.1:p.Pro136Arg
NM_213647.3:c.407C>G MANE Select	NP_998812.1:p.Pro136Arg
NM_001291980.2:c.407C>G	NP_001278909.1:p.Pro136Arg
NM_001354984.2:c.407C>G	NP_001341913.1:p.Pro136Arg
NM_002011.5:c.407C>G	NP_002002.3:p.Pro136Arg