Canonical Allele Identifier: CA447725178

Gene: FGFR4

Linked Data

• dbSNP Id: rs1323224382
• gnomAD v3: 5-177092696-G-A
• gnomAD v4: 5-177092696-G-A
• MyVariant Identifiers: chr5:g.176519697G>A (hg19) ; chr5:g.177092696G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177092696G>A , CM000667.2:g.177092696G>A	GRCh38
NC_000005.9:g.176519697G>A , CM000667.1:g.176519697G>A	GRCh37
NC_000005.8:g.176452303G>A	NCBI36
NG_012067.1:g.10777G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.969G>A MANE Select	ENSP00000292408.4:p.Val323=
ENST00000292408.8:c.969G>A	ENSP00000292408.4:p.Val323=
ENST00000393637.5:c.969G>A	ENSP00000377254.1:p.Val323=
ENST00000393648.6:c.969G>A	ENSP00000377259.2:p.Val323=
ENST00000502906.5:c.969G>A	ENSP00000424960.1:p.Val323=
ENST00000508139.1:n.273G>A
ENST00000509511.5:n.969G>A
NM_001291980.1:c.969G>A	NP_001278909.1:p.Val323=
NM_002011.4:c.969G>A	NP_002002.3:p.Val323=
NM_022963.3:c.969G>A	NP_075252.2:p.Val323=
NM_213647.2:c.969G>A	NP_998812.1:p.Val323=
XM_005265838.2:c.969G>A	XP_005265895.1:p.Val323=
XM_011534464.1:c.1062G>A	XP_011532766.1:p.Val354=
XM_011534465.1:c.651G>A	XP_011532767.1:p.Val217=
XR_941090.1:n.1014G>A
NM_001354984.1:c.969G>A	NP_001341913.1:p.Val323=
NM_213647.3:c.969G>A MANE Select	NP_998812.1:p.Val323=
NM_001291980.2:c.969G>A	NP_001278909.1:p.Val323=
NM_001354984.2:c.969G>A	NP_001341913.1:p.Val323=
NM_002011.5:c.969G>A	NP_002002.3:p.Val323=