Canonical Allele Identifier: CA2676681603
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177092707_177092713del , CM000667.2:g.177092707_177092713del GRCh38
NC_000005.9:g.176519708_176519714del , CM000667.1:g.176519708_176519714del GRCh37
NC_000005.8:g.176452314_176452320del NCBI36
NG_012067.1:g.10788_10794del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.980_986del MANE Select ENSP00000292408.4:p.Asp327AlafsTer?
ENST00000292408.8:c.980_986del ENSP00000292408.4:p.Asp327AlafsTer?
ENST00000393637.5:c.980_986del ENSP00000377254.1:p.Asp327AlafsTer?
ENST00000393648.6:c.980_986del ENSP00000377259.2:p.Asp327AlafsTer?
ENST00000502906.5:c.980_986del ENSP00000424960.1:p.Asp327AlafsTer?
ENST00000508139.1:n.284_290del
ENST00000509511.5:n.980_986del
NM_001291980.1:c.980_986del NP_001278909.1:p.Asp327AlafsTer?
NM_002011.4:c.980_986del NP_002002.3:p.Asp327AlafsTer?
NM_022963.3:c.980_986del NP_075252.2:p.Asp327AlafsTer?
NM_213647.2:c.980_986del NP_998812.1:p.Asp327AlafsTer?
XM_005265838.2:c.980_986del XP_005265895.1:p.Asp327AlafsTer?
XM_011534464.1:c.1073_1079del XP_011532766.1:p.Asp358AlafsTer?
XM_011534465.1:c.662_668del XP_011532767.1:p.Asp221AlafsTer?
XR_941090.1:n.1025_1031del
NM_001354984.1:c.980_986del NP_001341913.1:p.Asp327AlafsTer?
NM_213647.3:c.980_986del MANE Select NP_998812.1:p.Asp327AlafsTer?
NM_001291980.2:c.980_986del NP_001278909.1:p.Asp327AlafsTer?
NM_001354984.2:c.980_986del NP_001341913.1:p.Asp327AlafsTer?
NM_002011.5:c.980_986del NP_002002.3:p.Asp327AlafsTer?