Canonical Allele Identifier: CA438063265

Gene: FGFR3

Linked Data

• MyVariant Identifiers: chr4:g.1807894G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1806167G>T , CM000666.2:g.1806167G>T	GRCh38
NC_000004.11:g.1807894G>T , CM000666.1:g.1807894G>T	GRCh37
NC_000004.10:g.1777692G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000340107.9:c.1959G>T	ENSP00000339824.4:p.Thr653=
ENST00000260795.8:c.*1009G>T	ENSP00000260795.3:n.*1009G>T
ENST00000352904.6:c.1617G>T	ENSP00000231803.1:p.Thr539=
ENST00000412135.7:c.1941G>T	ENSP00000412903.3:p.Thr647=
ENST00000440486.8:c.1953G>T MANE Select	ENSP00000414914.2:p.Thr651=
ENST00000481110.7:c.1956G>T	ENSP00000420533.2:p.Thr652=
ENST00000260795.6:c.1953G>T	ENSP00000260795.2:p.Thr651=
ENST00000340107.8:c.1959G>T	ENSP00000339824.4:p.Thr653=
ENST00000352904.5:c.1617G>T	ENSP00000231803.1:p.Thr539=
ENST00000412135.6:c.1617G>T	ENSP00000412903.2:p.Thr539=
ENST00000440486.6:c.1953G>T	ENSP00000414914.2:p.Thr651=
ENST00000481110.6:c.1956G>T	ENSP00000420533.2:p.Thr652=
ENST00000613647.4:c.*1009G>T	ENSP00000479472.1:n.*1009G>T
XM_006713868.1:c.1965G>T	XP_006713931.1:p.Thr655=
XM_006713869.1:c.1965G>T	XP_006713932.1:p.Thr655=
XM_006713870.1:c.1962G>T	XP_006713933.1:p.Thr654=
XM_006713871.1:c.1959G>T	XP_006713934.1:p.Thr653=
XM_006713872.1:c.1956G>T	XP_006713935.1:p.Thr652=
XM_006713873.1:c.1953G>T	XP_006713936.1:p.Thr651=
XM_011513420.1:c.1959G>T	XP_011511722.1:p.Thr653=
XM_011513422.1:c.1956G>T	XP_011511724.1:p.Thr652=
NM_001354809.2:c.1956G>T	NP_001341738.1:p.Thr652=
NM_001354810.2:c.1956G>T	NP_001341739.1:p.Thr652=
NR_148971.2:n.2379G>T
NM_000142.5:c.1953G>T MANE Select	NP_000133.1:p.Thr651=
NM_001163213.2:c.1959G>T	NP_001156685.1:p.Thr653=
NM_022965.4:c.1617G>T	NP_075254.1:p.Thr539=