Canonical Allele Identifier: CA1603396981

Gene: FGFR4

Linked Data

• dbSNP Id: rs1784432240
• gnomAD v4: 5-177093258-AGGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093260_177093262del , CM000667.2:g.177093260_177093262del	GRCh38
NC_000005.9:g.176520261_176520263del , CM000667.1:g.176520261_176520263del	GRCh37
NC_000005.8:g.176452867_176452869del	NCBI36
NG_012067.1:g.11341_11343del

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.1180_1182del MANE Select	ENSP00000292408.4:p.Ala394del
ENST00000292408.8:c.1180_1182del	ENSP00000292408.4:p.Ala394del
ENST00000393637.5:c.1058-72_1058-70del	ENSP00000377254.1:n.1058-72_1058-70del
ENST00000393648.6:c.1097+83_1097+85del	ENSP00000377259.2:n.1097+83_1097+85del
ENST00000502906.5:c.1180_1182del	ENSP00000424960.1:p.Ala394del
ENST00000508139.1:n.484_486del
ENST00000511076.1:c.86_88del
NM_001291980.1:c.1097+83_1097+85del	NP_001278909.1:n.1097+83_1097+85del
NM_002011.4:c.1180_1182del	NP_002002.3:p.Ala394del
NM_022963.3:c.1058-72_1058-70del	NP_075252.2:n.1058-72_1058-70del
NM_213647.2:c.1180_1182del	NP_998812.1:p.Ala394del
XM_005265838.2:c.1180_1182del	XP_005265895.1:p.Ala394del
XM_011534464.1:c.1273_1275del	XP_011532766.1:p.Ala425del
XM_011534465.1:c.862_864del	XP_011532767.1:p.Ala288del
XR_941090.1:n.1225_1227del
NM_001354984.1:c.1180_1182del	NP_001341913.1:p.Ala394del
NM_213647.3:c.1180_1182del MANE Select	NP_998812.1:p.Ala394del
NM_001291980.2:c.1097+83_1097+85del	NP_001278909.1:n.1097+83_1097+85del
NM_001354984.2:c.1180_1182del	NP_001341913.1:p.Ala394del
NM_002011.5:c.1180_1182del	NP_002002.3:p.Ala394del