Canonical Allele Identifier: CA1433506755
Gene: FGFR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1804452A= , CM000666.2:g.1804452A= GRCh38
NC_000004.11:g.1806179A= , CM000666.1:g.1806179A= GRCh37
NC_000004.10:g.1775977A= NCBI36
NG_012632.1:g.16141A= , LRG_1021:g.16141A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340107.9:c.1204A= ENSP00000339824.4:p.Ser402=
ENST00000260795.8:c.*254A= ENSP00000260795.3:n.*254A=
ENST00000352904.6:c.931-372A= ENSP00000231803.1:n.931-372A=
ENST00000412135.7:c.1186A= ENSP00000412903.3:p.Ser396=
ENST00000440486.8:c.1198A= MANE Select ENSP00000414914.2:p.Ser400=
ENST00000481110.7:c.1198A= ENSP00000420533.2:p.Ser400=
ENST00000643463.1:n.349A=
ENST00000260795.6:c.1198A= ENSP00000260795.2:p.Ser400=
ENST00000340107.8:c.1204A= ENSP00000339824.4:p.Ser402=
ENST00000352904.5:c.931-372A= ENSP00000231803.1:n.931-372A=
ENST00000412135.6:c.931-372A= ENSP00000412903.2:n.931-372A=
ENST00000440486.6:c.1198A= ENSP00000414914.2:p.Ser400=
ENST00000481110.6:c.1198A= ENSP00000420533.2:p.Ser400=
ENST00000613647.4:c.*254A= ENSP00000479472.1:n.*254A=
NM_000142.4:c.1198A= , LRG_1021t1:c.1198A= NP_000133.1:p.Ser400=
NM_001163213.1:c.1204A= , LRG_1021t2:c.1204A= NP_001156685.1:p.Ser402=
NM_022965.3:c.931-372A= NP_075254.1:n.931-372A=
XM_006713868.1:c.1204A= XP_006713931.1:p.Ser402=
XM_006713869.1:c.1204A= XP_006713932.1:p.Ser402=
XM_006713870.1:c.1204A= XP_006713933.1:p.Ser402=
XM_006713871.1:c.1204A= XP_006713934.1:p.Ser402=
XM_006713872.1:c.1198A= XP_006713935.1:p.Ser400=
XM_006713873.1:c.1198A= XP_006713936.1:p.Ser400=
XM_011513420.1:c.1198A= XP_011511722.1:p.Ser400=
XM_011513422.1:c.1198A= XP_011511724.1:p.Ser400=
NM_001354809.1:c.1198A= NP_001341738.1:p.Ser400=
NM_001354810.1:c.1198A= NP_001341739.1:p.Ser400=
NR_148971.1:n.1605A=
NM_001354809.2:c.1198A= NP_001341738.1:p.Ser400=
NM_001354810.2:c.1198A= NP_001341739.1:p.Ser400=
NR_148971.2:n.1624A=
NM_000142.5:c.1198A= MANE Select NP_000133.1:p.Ser400=
NM_001163213.2:c.1204A= NP_001156685.1:p.Ser402=
NM_022965.4:c.931-372A= NP_075254.1:n.931-372A=