Canonical Allele Identifier: CA362291939
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs750129867

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093293A>C , CM000667.2:g.177093293A>C GRCh38
NC_000005.9:g.176520294A>C , CM000667.1:g.176520294A>C GRCh37
NC_000005.8:g.176452900A>C NCBI36
NG_012067.1:g.11374A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1213A>C MANE Select ENSP00000292408.4:p.Thr405Pro
ENST00000292408.8:c.1213A>C ENSP00000292408.4:p.Thr405Pro
ENST00000393637.5:c.1058-39A>C ENSP00000377254.1:n.1058-39A>C
ENST00000393648.6:c.1098-113A>C ENSP00000377259.2:n.1098-113A>C
ENST00000502906.5:c.1213A>C ENSP00000424960.1:p.Thr405Pro
ENST00000508139.1:n.517A>C
ENST00000511076.1:c.119A>C
NM_001291980.1:c.1098-113A>C NP_001278909.1:n.1098-113A>C
NM_002011.4:c.1213A>C NP_002002.3:p.Thr405Pro
NM_022963.3:c.1058-39A>C NP_075252.2:n.1058-39A>C
NM_213647.2:c.1213A>C NP_998812.1:p.Thr405Pro
XM_005265838.2:c.1213A>C XP_005265895.1:p.Thr405Pro
XM_011534464.1:c.1306A>C XP_011532766.1:p.Thr436Pro
XM_011534465.1:c.895A>C XP_011532767.1:p.Thr299Pro
XR_941090.1:n.1258A>C
NM_001354984.1:c.1213A>C NP_001341913.1:p.Thr405Pro
NM_213647.3:c.1213A>C MANE Select NP_998812.1:p.Thr405Pro
NM_001291980.2:c.1098-113A>C NP_001278909.1:n.1098-113A>C
NM_001354984.2:c.1213A>C NP_001341913.1:p.Thr405Pro
NM_002011.5:c.1213A>C NP_002002.3:p.Thr405Pro