Canonical Allele Identifier: CA1433506295
Gene: FGFR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1803725G= , CM000666.2:g.1803725G= GRCh38
NC_000004.11:g.1805452G= , CM000666.1:g.1805452G= GRCh37
NC_000004.10:g.1775250G= NCBI36
NG_012632.1:g.15414G= , LRG_1021:g.15414G=

Transcript Alleles

HGVS Amino-acid Change
NM_000142.5:c.964G= MANE Select NP_000133.1:p.Glu322=
ENST00000440486.8:c.964G= MANE Select ENSP00000414914.2:p.Glu322=
NM_000142.4:c.964G= , LRG_1021t1:c.964G= NP_000133.1:p.Glu322=
NM_001163213.1:c.1082-605G= , LRG_1021t2:c.1082-605G= NP_001156685.1:n.1082-605G=
NM_001163213.2:c.1082-605G= NP_001156685.1:n.1082-605G=
NM_001354809.1:c.964G= NP_001341738.1:p.Glu322=
NM_001354809.2:c.964G= NP_001341738.1:p.Glu322=
NM_001354810.1:c.964G= NP_001341739.1:p.Glu322=
NM_001354810.2:c.964G= NP_001341739.1:p.Glu322=
NM_022965.3:c.931-1099G= NP_075254.1:n.931-1099G=
NM_022965.4:c.931-1099G= NP_075254.1:n.931-1099G=
NR_148971.1:n.1371G=
NR_148971.2:n.1390G=
ENST00000260795.6:c.964G= ENSP00000260795.2:p.Glu322=
ENST00000260795.8:c.*20G= ENSP00000260795.3:n.*20G=
ENST00000340107.8:c.1082-605G= ENSP00000339824.4:n.1082-605G=
ENST00000340107.9:c.1082-605G= ENSP00000339824.4:n.1082-605G=
ENST00000352904.5:c.931-1099G= ENSP00000231803.1:n.931-1099G=
ENST00000352904.6:c.931-1099G= ENSP00000231803.1:n.931-1099G=
ENST00000412135.6:c.931-1099G= ENSP00000412903.2:n.931-1099G=
ENST00000412135.7:c.952G= ENSP00000412903.3:p.Glu318=
ENST00000440486.6:c.964G= ENSP00000414914.2:p.Glu322=
ENST00000481110.6:c.964G= ENSP00000420533.2:p.Glu322=
ENST00000481110.7:c.964G= ENSP00000420533.2:p.Glu322=
ENST00000507588.1:c.322G= ENSP00000427289.1:p.Glu108=
ENST00000613647.4:c.*20G= ENSP00000479472.1:n.*20G=
ENST00000643463.1:n.227-605G=
XM_006713868.1:c.1082-605G= XP_006713931.1:n.1082-605G=
XM_006713869.1:c.1082-605G= XP_006713932.1:n.1082-605G=
XM_006713870.1:c.1082-605G= XP_006713933.1:n.1082-605G=
XM_006713871.1:c.1082-605G= XP_006713934.1:n.1082-605G=
XM_006713872.1:c.964G= XP_006713935.1:p.Glu322=
XM_006713873.1:c.964G= XP_006713936.1:p.Glu322=
XM_011513420.1:c.964G= XP_011511722.1:p.Glu322=
XM_011513422.1:c.964G= XP_011511724.1:p.Glu322=