Canonical Allele Identifier: CA1603397452

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093539_177093540delinsTC , CM000667.2:g.177093539_177093540delinsTC	GRCh38
NC_000005.9:g.176520540_176520541delinsTC , CM000667.1:g.176520540_176520541delinsTC	GRCh37
NC_000005.8:g.176453146_176453147delinsTC	NCBI36
NG_012067.1:g.11620_11621delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1385_1386delinsTC MANE Select	ENSP00000292408.4:p.Phe462=
ENST00000292408.8:c.1385_1386delinsTC	ENSP00000292408.4:p.Phe462=
ENST00000393637.5:c.1265_1266delinsTC	ENSP00000377254.1:p.Phe422=
ENST00000393648.6:c.1193+38_1193+39delinsTC	ENSP00000377259.2:n.1193+38_1193+39delinsTC
ENST00000502906.5:c.1385_1386delinsTC	ENSP00000424960.1:p.Phe462=
ENST00000511076.1:c.279_280delinsTC
NM_001291980.1:c.1193+38_1193+39delinsTC	NP_001278909.1:n.1193+38_1193+39delinsTC
NM_002011.4:c.1385_1386delinsTC	NP_002002.3:p.Phe462=
NM_022963.3:c.1265_1266delinsTC	NP_075252.2:p.Phe422=
NM_213647.2:c.1385_1386delinsTC	NP_998812.1:p.Phe462=
XM_005265838.2:c.1385_1386delinsTC	XP_005265895.1:p.Phe462=
XM_011534464.1:c.1478_1479delinsTC	XP_011532766.1:p.Phe493=
XM_011534465.1:c.1067_1068delinsTC	XP_011532767.1:p.Phe356=
XR_941090.1:n.1392+38_1392+39delinsTC
NM_001354984.1:c.1385_1386delinsTC	NP_001341913.1:p.Phe462=
NM_213647.3:c.1385_1386delinsTC MANE Select	NP_998812.1:p.Phe462=
NM_001291980.2:c.1193+38_1193+39delinsTC	NP_001278909.1:n.1193+38_1193+39delinsTC
NM_001354984.2:c.1385_1386delinsTC	NP_001341913.1:p.Phe462=
NM_002011.5:c.1385_1386delinsTC	NP_002002.3:p.Phe462=