Canonical Allele Identifier: CA1433506722
Gene: FGFR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1804392G= , CM000666.2:g.1804392G= GRCh38
NC_000004.11:g.1806119G= , CM000666.1:g.1806119G= GRCh37
NC_000004.10:g.1775917G= NCBI36
NG_012632.1:g.16081G= , LRG_1021:g.16081G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340107.9:c.1144G= ENSP00000339824.4:p.Gly382=
ENST00000260795.8:c.*194G= ENSP00000260795.3:n.*194G=
ENST00000352904.6:c.931-432G= ENSP00000231803.1:n.931-432G=
ENST00000412135.7:c.1126G= ENSP00000412903.3:p.Gly376=
ENST00000440486.8:c.1138G= MANE Select ENSP00000414914.2:p.Gly380=
ENST00000481110.7:c.1138G= ENSP00000420533.2:p.Gly380=
ENST00000643463.1:n.289G=
ENST00000260795.6:c.1138G= ENSP00000260795.2:p.Gly380=
ENST00000340107.8:c.1144G= ENSP00000339824.4:p.Gly382=
ENST00000352904.5:c.931-432G= ENSP00000231803.1:n.931-432G=
ENST00000412135.6:c.931-432G= ENSP00000412903.2:n.931-432G=
ENST00000440486.6:c.1138G= ENSP00000414914.2:p.Gly380=
ENST00000481110.6:c.1138G= ENSP00000420533.2:p.Gly380=
ENST00000613647.4:c.*194G= ENSP00000479472.1:n.*194G=
NM_000142.4:c.1138G= , LRG_1021t1:c.1138G= NP_000133.1:p.Gly380=
NM_001163213.1:c.1144G= , LRG_1021t2:c.1144G= NP_001156685.1:p.Gly382=
NM_022965.3:c.931-432G= NP_075254.1:n.931-432G=
XM_006713868.1:c.1144G= XP_006713931.1:p.Gly382=
XM_006713869.1:c.1144G= XP_006713932.1:p.Gly382=
XM_006713870.1:c.1144G= XP_006713933.1:p.Gly382=
XM_006713871.1:c.1144G= XP_006713934.1:p.Gly382=
XM_006713872.1:c.1138G= XP_006713935.1:p.Gly380=
XM_006713873.1:c.1138G= XP_006713936.1:p.Gly380=
XM_011513420.1:c.1138G= XP_011511722.1:p.Gly380=
XM_011513422.1:c.1138G= XP_011511724.1:p.Gly380=
NM_001354809.1:c.1138G= NP_001341738.1:p.Gly380=
NM_001354810.1:c.1138G= NP_001341739.1:p.Gly380=
NR_148971.1:n.1545G=
NM_001354809.2:c.1138G= NP_001341738.1:p.Gly380=
NM_001354810.2:c.1138G= NP_001341739.1:p.Gly380=
NR_148971.2:n.1564G=
NM_000142.5:c.1138G= MANE Select NP_000133.1:p.Gly380=
NM_001163213.2:c.1144G= NP_001156685.1:p.Gly382=
NM_022965.4:c.931-432G= NP_075254.1:n.931-432G=