Canonical Allele Identifier: CA2676680987

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177090800-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177090802del , CM000667.2:g.177090802del	GRCh38
NC_000005.9:g.176517803del , CM000667.1:g.176517803del	GRCh37
NC_000005.8:g.176450409del	NCBI36
NG_012067.1:g.8883del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.413del MANE Select	ENSP00000292408.4:p.Asn138IlefsTer?
ENST00000292408.8:c.413del	ENSP00000292408.4:p.Asn138IlefsTer?
ENST00000393637.5:c.413del	ENSP00000377254.1:p.Asn138IlefsTer?
ENST00000393648.6:c.413del	ENSP00000377259.2:p.Asn138IlefsTer?
ENST00000426612.5:n.418del
ENST00000430285.5:c.*277del	ENSP00000395164.1:n.*277del
ENST00000502906.5:c.413del	ENSP00000424960.1:p.Asn138IlefsTer?
ENST00000503708.5:c.413del	ENSP00000424905.1:p.Asn138IlefsTer?
ENST00000509511.5:n.413del
NM_001291980.1:c.413del	NP_001278909.1:p.Asn138IlefsTer?
NM_002011.4:c.413del	NP_002002.3:p.Asn138IlefsTer?
NM_022963.3:c.413del	NP_075252.2:p.Asn138IlefsTer?
NM_213647.2:c.413del	NP_998812.1:p.Asn138IlefsTer?
XM_005265838.2:c.413del	XP_005265895.1:p.Asn138IlefsTer?
XM_011534464.1:c.506del	XP_011532766.1:p.Asn169IlefsTer?
XM_011534465.1:c.95del	XP_011532767.1:p.Asn32IlefsTer?
XR_941090.1:n.458del
NM_001354984.1:c.413del	NP_001341913.1:p.Asn138IlefsTer?
NM_213647.3:c.413del MANE Select	NP_998812.1:p.Asn138IlefsTer?
NM_001291980.2:c.413del	NP_001278909.1:p.Asn138IlefsTer?
NM_001354984.2:c.413del	NP_001341913.1:p.Asn138IlefsTer?
NM_002011.5:c.413del	NP_002002.3:p.Asn138IlefsTer?