Canonical Allele Identifier: CA362291465
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs1250996076

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093246T>C , CM000667.2:g.177093246T>C GRCh38
NC_000005.9:g.176520247T>C , CM000667.1:g.176520247T>C GRCh37
NC_000005.8:g.176452853T>C NCBI36
NG_012067.1:g.11327T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000292408.9:c.1166T>C MANE Select ENSP00000292408.4:p.Leu389Pro
ENST00000292408.8:c.1166T>C ENSP00000292408.4:p.Leu389Pro
ENST00000393637.5:c.1058-86T>C ENSP00000377254.1:n.1058-86T>C
ENST00000393648.6:c.1097+69T>C ENSP00000377259.2:n.1097+69T>C
ENST00000502906.5:c.1166T>C ENSP00000424960.1:p.Leu389Pro
ENST00000508139.1:n.470T>C
ENST00000511076.1:c.72T>C
NM_001291980.1:c.1097+69T>C NP_001278909.1:n.1097+69T>C
NM_002011.4:c.1166T>C NP_002002.3:p.Leu389Pro
NM_022963.3:c.1058-86T>C NP_075252.2:n.1058-86T>C
NM_213647.2:c.1166T>C NP_998812.1:p.Leu389Pro
XM_005265838.2:c.1166T>C XP_005265895.1:p.Leu389Pro
XM_011534464.1:c.1259T>C XP_011532766.1:p.Leu420Pro
XM_011534465.1:c.848T>C XP_011532767.1:p.Leu283Pro
XR_941090.1:n.1211T>C
NM_001354984.1:c.1166T>C NP_001341913.1:p.Leu389Pro
NM_213647.3:c.1166T>C MANE Select NP_998812.1:p.Leu389Pro
NM_001291980.2:c.1097+69T>C NP_001278909.1:n.1097+69T>C
NM_001354984.2:c.1166T>C NP_001341913.1:p.Leu389Pro
NM_002011.5:c.1166T>C NP_002002.3:p.Leu389Pro