Canonical Allele Identifier: CA3576037

Gene: FGFR4

Linked Data

• ClinVar Variation Id: 3048070
• ClinVar RCV Id: RCV003951892
• dbSNP Id: rs55675160
• ExAC: 5:176518037 A / G
• gnomAD v2: 5-176518037-A-G
• gnomAD v3: 5-177091036-A-G
• gnomAD v4: 5-177091036-A-G
• MyVariant Identifiers: chr5:g.176518037A>G (hg19) ; chr5:g.177091036A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177091036A>G , CM000667.2:g.177091036A>G	GRCh38
NC_000005.9:g.176518037A>G , CM000667.1:g.176518037A>G	GRCh37
NC_000005.8:g.176450643A>G	NCBI36
NG_012067.1:g.9117A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.535A>G MANE Select	ENSP00000292408.4:p.Thr179Ala
ENST00000292408.8:c.535A>G	ENSP00000292408.4:p.Thr179Ala
ENST00000393637.5:c.535A>G	ENSP00000377254.1:p.Thr179Ala
ENST00000393648.6:c.535A>G	ENSP00000377259.2:p.Thr179Ala
ENST00000426612.5:n.652A>G
ENST00000430285.5:c.*399A>G	ENSP00000395164.1:n.*399A>G
ENST00000502906.5:c.535A>G	ENSP00000424960.1:p.Thr179Ala
ENST00000503708.5:c.535A>G	ENSP00000424905.1:p.Thr179Ala
ENST00000509511.5:n.535A>G
NM_001291980.1:c.535A>G	NP_001278909.1:p.Thr179Ala
NM_002011.4:c.535A>G	NP_002002.3:p.Thr179Ala
NM_022963.3:c.535A>G	NP_075252.2:p.Thr179Ala
NM_213647.2:c.535A>G	NP_998812.1:p.Thr179Ala
XM_005265838.2:c.535A>G	XP_005265895.1:p.Thr179Ala
XM_011534464.1:c.628A>G	XP_011532766.1:p.Thr210Ala
XM_011534465.1:c.217A>G	XP_011532767.1:p.Thr73Ala
XR_941090.1:n.580A>G
NM_001354984.1:c.535A>G	NP_001341913.1:p.Thr179Ala
NM_213647.3:c.535A>G MANE Select	NP_998812.1:p.Thr179Ala
NM_001291980.2:c.535A>G	NP_001278909.1:p.Thr179Ala
NM_001354984.2:c.535A>G	NP_001341913.1:p.Thr179Ala
NM_002011.5:c.535A>G	NP_002002.3:p.Thr179Ala