Canonical Allele Identifier: CA3576381
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs374011645

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093547G>T , CM000667.2:g.177093547G>T GRCh38
NC_000005.9:g.176520548G>T , CM000667.1:g.176520548G>T GRCh37
NC_000005.8:g.176453154G>T NCBI36
NG_012067.1:g.11628G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1393G>T MANE Select ENSP00000292408.4:p.Asp465Tyr
ENST00000292408.8:c.1393G>T ENSP00000292408.4:p.Asp465Tyr
ENST00000393637.5:c.1273G>T ENSP00000377254.1:p.Asp425Tyr
ENST00000393648.6:c.1193+46G>T ENSP00000377259.2:n.1193+46G>T
ENST00000502906.5:c.1393G>T ENSP00000424960.1:p.Asp465Tyr
ENST00000511076.1:c.287G>T
NM_001291980.1:c.1193+46G>T NP_001278909.1:n.1193+46G>T
NM_002011.4:c.1393G>T NP_002002.3:p.Asp465Tyr
NM_022963.3:c.1273G>T NP_075252.2:p.Asp425Tyr
NM_213647.2:c.1393G>T NP_998812.1:p.Asp465Tyr
XM_005265838.2:c.1393G>T XP_005265895.1:p.Asp465Tyr
XM_011534464.1:c.1486G>T XP_011532766.1:p.Asp496Tyr
XM_011534465.1:c.1075G>T XP_011532767.1:p.Asp359Tyr
XR_941090.1:n.1392+46G>T
NM_001354984.1:c.1393G>T NP_001341913.1:p.Asp465Tyr
NM_213647.3:c.1393G>T MANE Select NP_998812.1:p.Asp465Tyr
NM_001291980.2:c.1193+46G>T NP_001278909.1:n.1193+46G>T
NM_001354984.2:c.1393G>T NP_001341913.1:p.Asp465Tyr
NM_002011.5:c.1393G>T NP_002002.3:p.Asp465Tyr