Canonical Allele Identifier: CA1433506739
Gene: FGFR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1804416C= , CM000666.2:g.1804416C= GRCh38
NC_000004.11:g.1806143C= , CM000666.1:g.1806143C= GRCh37
NC_000004.10:g.1775941C= NCBI36
NG_012632.1:g.16105C= , LRG_1021:g.16105C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340107.9:c.1168C= ENSP00000339824.4:p.Leu390=
ENST00000260795.8:c.*218C= ENSP00000260795.3:n.*218C=
ENST00000352904.6:c.931-408C= ENSP00000231803.1:n.931-408C=
ENST00000412135.7:c.1150C= ENSP00000412903.3:p.Leu384=
ENST00000440486.8:c.1162C= MANE Select ENSP00000414914.2:p.Leu388=
ENST00000481110.7:c.1162C= ENSP00000420533.2:p.Leu388=
ENST00000643463.1:n.313C=
ENST00000260795.6:c.1162C= ENSP00000260795.2:p.Leu388=
ENST00000340107.8:c.1168C= ENSP00000339824.4:p.Leu390=
ENST00000352904.5:c.931-408C= ENSP00000231803.1:n.931-408C=
ENST00000412135.6:c.931-408C= ENSP00000412903.2:n.931-408C=
ENST00000440486.6:c.1162C= ENSP00000414914.2:p.Leu388=
ENST00000481110.6:c.1162C= ENSP00000420533.2:p.Leu388=
ENST00000613647.4:c.*218C= ENSP00000479472.1:n.*218C=
NM_000142.4:c.1162C= , LRG_1021t1:c.1162C= NP_000133.1:p.Leu388=
NM_001163213.1:c.1168C= , LRG_1021t2:c.1168C= NP_001156685.1:p.Leu390=
NM_022965.3:c.931-408C= NP_075254.1:n.931-408C=
XM_006713868.1:c.1168C= XP_006713931.1:p.Leu390=
XM_006713869.1:c.1168C= XP_006713932.1:p.Leu390=
XM_006713870.1:c.1168C= XP_006713933.1:p.Leu390=
XM_006713871.1:c.1168C= XP_006713934.1:p.Leu390=
XM_006713872.1:c.1162C= XP_006713935.1:p.Leu388=
XM_006713873.1:c.1162C= XP_006713936.1:p.Leu388=
XM_011513420.1:c.1162C= XP_011511722.1:p.Leu388=
XM_011513422.1:c.1162C= XP_011511724.1:p.Leu388=
NM_001354809.1:c.1162C= NP_001341738.1:p.Leu388=
NM_001354810.1:c.1162C= NP_001341739.1:p.Leu388=
NR_148971.1:n.1569C=
NM_001354809.2:c.1162C= NP_001341738.1:p.Leu388=
NM_001354810.2:c.1162C= NP_001341739.1:p.Leu388=
NR_148971.2:n.1588C=
NM_000142.5:c.1162C= MANE Select NP_000133.1:p.Leu388=
NM_001163213.2:c.1168C= NP_001156685.1:p.Leu390=
NM_022965.4:c.931-408C= NP_075254.1:n.931-408C=