Canonical Allele Identifier: CA3576375

Gene: FGFR4

Linked Data

• dbSNP Id: rs552027908
• ExAC: 5:176520539 T / A
• gnomAD v2: 5-176520539-T-A
• gnomAD v3: 5-177093538-T-A
• gnomAD v4: 5-177093538-T-A
• MyVariant Identifiers: chr5:g.176520539T>A (hg19) ; chr5:g.177093538T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093538T>A , CM000667.2:g.177093538T>A	GRCh38
NC_000005.9:g.176520539T>A , CM000667.1:g.176520539T>A	GRCh37
NC_000005.8:g.176453145T>A	NCBI36
NG_012067.1:g.11619T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1384T>A MANE Select	ENSP00000292408.4:p.Phe462Ile
ENST00000292408.8:c.1384T>A	ENSP00000292408.4:p.Phe462Ile
ENST00000393637.5:c.1264T>A	ENSP00000377254.1:p.Phe422Ile
ENST00000393648.6:c.1193+37T>A	ENSP00000377259.2:n.1193+37T>A
ENST00000502906.5:c.1384T>A	ENSP00000424960.1:p.Phe462Ile
ENST00000511076.1:c.278T>A
NM_001291980.1:c.1193+37T>A	NP_001278909.1:n.1193+37T>A
NM_002011.4:c.1384T>A	NP_002002.3:p.Phe462Ile
NM_022963.3:c.1264T>A	NP_075252.2:p.Phe422Ile
NM_213647.2:c.1384T>A	NP_998812.1:p.Phe462Ile
XM_005265838.2:c.1384T>A	XP_005265895.1:p.Phe462Ile
XM_011534464.1:c.1477T>A	XP_011532766.1:p.Phe493Ile
XM_011534465.1:c.1066T>A	XP_011532767.1:p.Phe356Ile
XR_941090.1:n.1392+37T>A
NM_001354984.1:c.1384T>A	NP_001341913.1:p.Phe462Ile
NM_213647.3:c.1384T>A MANE Select	NP_998812.1:p.Phe462Ile
NM_001291980.2:c.1193+37T>A	NP_001278909.1:n.1193+37T>A
NM_001354984.2:c.1384T>A	NP_001341913.1:p.Phe462Ile
NM_002011.5:c.1384T>A	NP_002002.3:p.Phe462Ile