Canonical Allele Identifier: CA1433507535
Gene: FGFR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1805661C= , CM000666.2:g.1805661C= GRCh38
NC_000004.11:g.1807388C= , CM000666.1:g.1807388C= GRCh37
NC_000004.10:g.1777186C= NCBI36
NG_012632.1:g.17350C= , LRG_1021:g.17350C=

Transcript Alleles

HGVS Amino-acid Change
NM_000142.5:c.1637C= MANE Select NP_000133.1:p.Thr546=
ENST00000440486.8:c.1637C= MANE Select ENSP00000414914.2:p.Thr546=
NM_000142.4:c.1637C= , LRG_1021t1:c.1637C= NP_000133.1:p.Thr546=
NM_001163213.1:c.1643C= , LRG_1021t2:c.1643C= NP_001156685.1:p.Thr548=
NM_001163213.2:c.1643C= NP_001156685.1:p.Thr548=
NM_001354809.1:c.1640C= NP_001341738.1:p.Thr547=
NM_001354809.2:c.1640C= NP_001341738.1:p.Thr547=
NM_001354810.1:c.1640C= NP_001341739.1:p.Thr547=
NM_001354810.2:c.1640C= NP_001341739.1:p.Thr547=
NM_022965.3:c.1301C= NP_075254.1:p.Thr434=
NM_022965.4:c.1301C= NP_075254.1:p.Thr434=
NR_148971.1:n.2044C=
NR_148971.2:n.2063C=
ENST00000260795.6:c.1637C= ENSP00000260795.2:p.Thr546=
ENST00000260795.8:c.*693C= ENSP00000260795.3:n.*693C=
ENST00000340107.8:c.1643C= ENSP00000339824.4:p.Thr548=
ENST00000340107.9:c.1643C= ENSP00000339824.4:p.Thr548=
ENST00000352904.5:c.1301C= ENSP00000231803.1:p.Thr434=
ENST00000352904.6:c.1301C= ENSP00000231803.1:p.Thr434=
ENST00000412135.6:c.1301C= ENSP00000412903.2:p.Thr434=
ENST00000412135.7:c.1625C= ENSP00000412903.3:p.Thr542=
ENST00000440486.6:c.1637C= ENSP00000414914.2:p.Thr546=
ENST00000469068.1:n.703C=
ENST00000481110.6:c.1640C= ENSP00000420533.2:p.Thr547=
ENST00000481110.7:c.1640C= ENSP00000420533.2:p.Thr547=
ENST00000613647.4:c.*693C= ENSP00000479472.1:n.*693C=
XM_006713868.1:c.1649C= XP_006713931.1:p.Thr550=
XM_006713869.1:c.1649C= XP_006713932.1:p.Thr550=
XM_006713870.1:c.1646C= XP_006713933.1:p.Thr549=
XM_006713871.1:c.1643C= XP_006713934.1:p.Thr548=
XM_006713872.1:c.1640C= XP_006713935.1:p.Thr547=
XM_006713873.1:c.1637C= XP_006713936.1:p.Thr546=
XM_011513420.1:c.1643C= XP_011511722.1:p.Thr548=
XM_011513422.1:c.1640C= XP_011511724.1:p.Thr547=