Canonical Allele Identifier: CA3576772
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs192201146

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177097533G>A , CM000667.2:g.177097533G>A GRCh38
NC_000005.9:g.176524534G>A , CM000667.1:g.176524534G>A GRCh37
NC_000005.8:g.176457140G>A NCBI36
NG_012067.1:g.15614G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000292408.9:c.2266G>A MANE Select ENSP00000292408.4:p.Asp756Asn
ENST00000292408.8:c.2266G>A ENSP00000292408.4:p.Asp756Asn
ENST00000393637.5:c.2146G>A ENSP00000377254.1:p.Asp716Asn
ENST00000393648.6:c.2062G>A ENSP00000377259.2:p.Asp688Asn
ENST00000502906.5:c.2266G>A ENSP00000424960.1:p.Asp756Asn
ENST00000513423.1:n.214G>A
NM_001291980.1:c.2062G>A NP_001278909.1:p.Asp688Asn
NM_002011.4:c.2266G>A NP_002002.3:p.Asp756Asn
NM_022963.3:c.2146G>A NP_075252.2:p.Asp716Asn
NM_213647.2:c.2266G>A NP_998812.1:p.Asp756Asn
XM_005265838.2:c.2266G>A XP_005265895.1:p.Asp756Asn
XM_011534464.1:c.2359G>A XP_011532766.1:p.Asp787Asn
XM_011534465.1:c.1948G>A XP_011532767.1:p.Asp650Asn
NM_001354984.1:c.2266G>A NP_001341913.1:p.Asp756Asn
NM_213647.3:c.2266G>A MANE Select NP_998812.1:p.Asp756Asn
NM_001291980.2:c.2062G>A NP_001278909.1:p.Asp688Asn
NM_001354984.2:c.2266G>A NP_001341913.1:p.Asp756Asn
NM_002011.5:c.2266G>A NP_002002.3:p.Asp756Asn