Canonical Allele Identifier: CA3576290
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs745448444

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093247G>A , CM000667.2:g.177093247G>A GRCh38
NC_000005.9:g.176520248G>A , CM000667.1:g.176520248G>A GRCh37
NC_000005.8:g.176452854G>A NCBI36
NG_012067.1:g.11328G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000292408.9:c.1167G>A MANE Select ENSP00000292408.4:p.Leu389=
ENST00000292408.8:c.1167G>A ENSP00000292408.4:p.Leu389=
ENST00000393637.5:c.1058-85G>A ENSP00000377254.1:n.1058-85G>A
ENST00000393648.6:c.1097+70G>A ENSP00000377259.2:n.1097+70G>A
ENST00000502906.5:c.1167G>A ENSP00000424960.1:p.Leu389=
ENST00000508139.1:n.471G>A
ENST00000511076.1:c.73G>A
NM_001291980.1:c.1097+70G>A NP_001278909.1:n.1097+70G>A
NM_002011.4:c.1167G>A NP_002002.3:p.Leu389=
NM_022963.3:c.1058-85G>A NP_075252.2:n.1058-85G>A
NM_213647.2:c.1167G>A NP_998812.1:p.Leu389=
XM_005265838.2:c.1167G>A XP_005265895.1:p.Leu389=
XM_011534464.1:c.1260G>A XP_011532766.1:p.Leu420=
XM_011534465.1:c.849G>A XP_011532767.1:p.Leu283=
XR_941090.1:n.1212G>A
NM_001354984.1:c.1167G>A NP_001341913.1:p.Leu389=
NM_213647.3:c.1167G>A MANE Select NP_998812.1:p.Leu389=
NM_001291980.2:c.1097+70G>A NP_001278909.1:n.1097+70G>A
NM_001354984.2:c.1167G>A NP_001341913.1:p.Leu389=
NM_002011.5:c.1167G>A NP_002002.3:p.Leu389=