Canonical Allele Identifier: CA1603404260
Gene: FGFR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177095470G= , CM000667.2:g.177095470G= GRCh38
NC_000005.9:g.176522471G= , CM000667.1:g.176522471G= GRCh37
NC_000005.8:g.176455077G= NCBI36
NG_012067.1:g.13551G=

Transcript Alleles

HGVS Amino-acid change
ENST00000292408.9:c.1630+30G= MANE Select ENSP00000292408.4:n.1630+30G=
ENST00000292408.8:c.1630+30G= ENSP00000292408.4:n.1630+30G=
ENST00000393637.5:c.1510+30G= ENSP00000377254.1:n.1510+30G=
ENST00000393648.6:c.1426+30G= ENSP00000377259.2:n.1426+30G=
ENST00000483872.2:n.616+30G=
ENST00000502906.5:c.1630+30G= ENSP00000424960.1:n.1630+30G=
ENST00000511076.1:c.524+30G=
NM_001291980.1:c.1426+30G= NP_001278909.1:n.1426+30G=
NM_002011.4:c.1630+30G= NP_002002.3:n.1630+30G=
NM_022963.3:c.1510+30G= NP_075252.2:n.1510+30G=
NM_213647.2:c.1630+30G= NP_998812.1:n.1630+30G=
XM_005265838.2:c.1630+30G= XP_005265895.1:n.1630+30G=
XM_011534464.1:c.1723+30G= XP_011532766.1:n.1723+30G=
XM_011534465.1:c.1312+30G= XP_011532767.1:n.1312+30G=
XR_941090.1:n.1625+30G=
NM_001354984.1:c.1630+30G= NP_001341913.1:n.1630+30G=
NM_213647.3:c.1630+30G= MANE Select NP_998812.1:n.1630+30G=
NM_001291980.2:c.1426+30G= NP_001278909.1:n.1426+30G=
NM_001354984.2:c.1630+30G= NP_001341913.1:n.1630+30G=
NM_002011.5:c.1630+30G= NP_002002.3:n.1630+30G=