Canonical Allele Identifier: CA3576379

Gene: FGFR4

Linked Data

• dbSNP Id: rs752246420
• ExAC: 5:176520546 G / A
• gnomAD v2: 5-176520546-G-A
• gnomAD v3: 5-177093545-G-A
• gnomAD v4: 5-177093545-G-A
• MyVariant Identifiers: chr5:g.176520546G>A (hg19) ; chr5:g.177093545G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093545G>A , CM000667.2:g.177093545G>A	GRCh38
NC_000005.9:g.176520546G>A , CM000667.1:g.176520546G>A	GRCh37
NC_000005.8:g.176453152G>A	NCBI36
NG_012067.1:g.11626G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1391G>A MANE Select	ENSP00000292408.4:p.Arg464Gln
ENST00000292408.8:c.1391G>A	ENSP00000292408.4:p.Arg464Gln
ENST00000393637.5:c.1271G>A	ENSP00000377254.1:p.Arg424Gln
ENST00000393648.6:c.1193+44G>A	ENSP00000377259.2:n.1193+44G>A
ENST00000502906.5:c.1391G>A	ENSP00000424960.1:p.Arg464Gln
ENST00000511076.1:c.285G>A
NM_001291980.1:c.1193+44G>A	NP_001278909.1:n.1193+44G>A
NM_002011.4:c.1391G>A	NP_002002.3:p.Arg464Gln
NM_022963.3:c.1271G>A	NP_075252.2:p.Arg424Gln
NM_213647.2:c.1391G>A	NP_998812.1:p.Arg464Gln
XM_005265838.2:c.1391G>A	XP_005265895.1:p.Arg464Gln
XM_011534464.1:c.1484G>A	XP_011532766.1:p.Arg495Gln
XM_011534465.1:c.1073G>A	XP_011532767.1:p.Arg358Gln
XR_941090.1:n.1392+44G>A
NM_001354984.1:c.1391G>A	NP_001341913.1:p.Arg464Gln
NM_213647.3:c.1391G>A MANE Select	NP_998812.1:p.Arg464Gln
NM_001291980.2:c.1193+44G>A	NP_001278909.1:n.1193+44G>A
NM_001354984.2:c.1391G>A	NP_001341913.1:p.Arg464Gln
NM_002011.5:c.1391G>A	NP_002002.3:p.Arg464Gln