Canonical Allele Identifier: CA362291775

Gene: FGFR4

Linked Data

• dbSNP Id: rs1270255483
• gnomAD v2: 5-176520271-G-A
• gnomAD v4: 5-177093270-G-A
• MyVariant Identifiers: chr5:g.176520271G>A (hg19) ; chr5:g.177093270G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093270G>A , CM000667.2:g.177093270G>A	GRCh38
NC_000005.9:g.176520271G>A , CM000667.1:g.176520271G>A	GRCh37
NC_000005.8:g.176452877G>A	NCBI36
NG_012067.1:g.11351G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.1190G>A MANE Select	ENSP00000292408.4:p.Gly397Asp
ENST00000292408.8:c.1190G>A	ENSP00000292408.4:p.Gly397Asp
ENST00000393637.5:c.1058-62G>A	ENSP00000377254.1:n.1058-62G>A
ENST00000393648.6:c.1097+93G>A	ENSP00000377259.2:n.1097+93G>A
ENST00000502906.5:c.1190G>A	ENSP00000424960.1:p.Gly397Asp
ENST00000508139.1:n.494G>A
ENST00000511076.1:c.96G>A
NM_001291980.1:c.1097+93G>A	NP_001278909.1:n.1097+93G>A
NM_002011.4:c.1190G>A	NP_002002.3:p.Gly397Asp
NM_022963.3:c.1058-62G>A	NP_075252.2:n.1058-62G>A
NM_213647.2:c.1190G>A	NP_998812.1:p.Gly397Asp
XM_005265838.2:c.1190G>A	XP_005265895.1:p.Gly397Asp
XM_011534464.1:c.1283G>A	XP_011532766.1:p.Gly428Asp
XM_011534465.1:c.872G>A	XP_011532767.1:p.Gly291Asp
XR_941090.1:n.1235G>A
NM_001354984.1:c.1190G>A	NP_001341913.1:p.Gly397Asp
NM_213647.3:c.1190G>A MANE Select	NP_998812.1:p.Gly397Asp
NM_001291980.2:c.1097+93G>A	NP_001278909.1:n.1097+93G>A
NM_001354984.2:c.1190G>A	NP_001341913.1:p.Gly397Asp
NM_002011.5:c.1190G>A	NP_002002.3:p.Gly397Asp