Canonical Allele Identifier: CA355975582
Gene: FGFR3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1801688C>A , CM000666.2:g.1801688C>A GRCh38
NC_000004.11:g.1803415C>A , CM000666.1:g.1803415C>A GRCh37
NC_000004.10:g.1773213C>A NCBI36
NG_012632.1:g.13377C>A , LRG_1021:g.13377C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000340107.9:c.684C>A ENSP00000339824.4:p.Cys228Ter
ENST00000260795.8:c.684C>A ENSP00000260795.3:p.Cys228Ter
ENST00000352904.6:c.684C>A ENSP00000231803.1:p.Cys228Ter
ENST00000412135.7:c.672C>A ENSP00000412903.3:p.Cys224Ter
ENST00000440486.8:c.684C>A MANE Select ENSP00000414914.2:p.Cys228Ter
ENST00000481110.7:c.684C>A ENSP00000420533.2:p.Cys228Ter
ENST00000260795.6:c.684C>A ENSP00000260795.2:p.Cys228Ter
ENST00000340107.8:c.684C>A ENSP00000339824.4:p.Cys228Ter
ENST00000352904.5:c.684C>A ENSP00000231803.1:p.Cys228Ter
ENST00000412135.6:c.684C>A ENSP00000412903.2:p.Cys228Ter
ENST00000440486.6:c.684C>A ENSP00000414914.2:p.Cys228Ter
ENST00000474521.1:n.60C>A
ENST00000481110.6:c.684C>A ENSP00000420533.2:p.Cys228Ter
ENST00000507588.1:c.144C>A ENSP00000427289.1:p.Cys48Ter
ENST00000613647.4:c.684C>A ENSP00000479472.1:p.Cys228Ter
NM_000142.4:c.684C>A , LRG_1021t1:c.684C>A NP_000133.1:p.Cys228Ter
NM_001163213.1:c.684C>A , LRG_1021t2:c.684C>A NP_001156685.1:p.Cys228Ter
NM_022965.3:c.684C>A NP_075254.1:p.Cys228Ter
XM_006713868.1:c.684C>A XP_006713931.1:p.Cys228Ter
XM_006713869.1:c.684C>A XP_006713932.1:p.Cys228Ter
XM_006713870.1:c.684C>A XP_006713933.1:p.Cys228Ter
XM_006713871.1:c.684C>A XP_006713934.1:p.Cys228Ter
XM_006713872.1:c.684C>A XP_006713935.1:p.Cys228Ter
XM_006713873.1:c.684C>A XP_006713936.1:p.Cys228Ter
XM_011513420.1:c.684C>A XP_011511722.1:p.Cys228Ter
XM_011513422.1:c.684C>A XP_011511724.1:p.Cys228Ter
NM_001354809.1:c.684C>A NP_001341738.1:p.Cys228Ter
NM_001354810.1:c.684C>A NP_001341739.1:p.Cys228Ter
NR_148971.1:n.940C>A
NM_001354809.2:c.684C>A NP_001341738.1:p.Cys228Ter
NM_001354810.2:c.684C>A NP_001341739.1:p.Cys228Ter
NR_148971.2:n.959C>A
NM_000142.5:c.684C>A MANE Select NP_000133.1:p.Cys228Ter
NM_001163213.2:c.684C>A NP_001156685.1:p.Cys228Ter
NM_022965.4:c.684C>A NP_075254.1:p.Cys228Ter