Canonical Allele Identifier: CA355981042

Gene: FGFR3

Linked Data

• MyVariant Identifiers: chr4:g.1807144T>C (hg19) ; chr4:g.1805417T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805417T>C , CM000666.2:g.1805417T>C	GRCh38
NC_000004.11:g.1807144T>C , CM000666.1:g.1807144T>C	GRCh37
NC_000004.10:g.1776942T>C	NCBI36
NG_012632.1:g.17106T>C , LRG_1021:g.17106T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1481T>C	ENSP00000339824.4:p.Ile494Thr
ENST00000260795.8:c.*531T>C	ENSP00000260795.3:n.*531T>C
ENST00000352904.6:c.1139T>C	ENSP00000231803.1:p.Ile380Thr
ENST00000412135.7:c.1463T>C	ENSP00000412903.3:p.Ile488Thr
ENST00000440486.8:c.1475T>C MANE Select	ENSP00000414914.2:p.Ile492Thr
ENST00000481110.7:c.1478T>C	ENSP00000420533.2:p.Ile493Thr
ENST00000260795.6:c.1475T>C	ENSP00000260795.2:p.Ile492Thr
ENST00000340107.8:c.1481T>C	ENSP00000339824.4:p.Ile494Thr
ENST00000352904.5:c.1139T>C	ENSP00000231803.1:p.Ile380Thr
ENST00000412135.6:c.1139T>C	ENSP00000412903.2:p.Ile380Thr
ENST00000440486.6:c.1475T>C	ENSP00000414914.2:p.Ile492Thr
ENST00000469068.1:n.541T>C
ENST00000481110.6:c.1478T>C	ENSP00000420533.2:p.Ile493Thr
ENST00000613647.4:c.*531T>C	ENSP00000479472.1:n.*531T>C
NM_000142.4:c.1475T>C , LRG_1021t1:c.1475T>C	NP_000133.1:p.Ile492Thr
NM_001163213.1:c.1481T>C , LRG_1021t2:c.1481T>C	NP_001156685.1:p.Ile494Thr
NM_022965.3:c.1139T>C	NP_075254.1:p.Ile380Thr
XM_006713868.1:c.1487T>C	XP_006713931.1:p.Ile496Thr
XM_006713869.1:c.1487T>C	XP_006713932.1:p.Ile496Thr
XM_006713870.1:c.1484T>C	XP_006713933.1:p.Ile495Thr
XM_006713871.1:c.1481T>C	XP_006713934.1:p.Ile494Thr
XM_006713872.1:c.1478T>C	XP_006713935.1:p.Ile493Thr
XM_006713873.1:c.1475T>C	XP_006713936.1:p.Ile492Thr
XM_011513420.1:c.1481T>C	XP_011511722.1:p.Ile494Thr
XM_011513422.1:c.1478T>C	XP_011511724.1:p.Ile493Thr
NM_001354809.1:c.1478T>C	NP_001341738.1:p.Ile493Thr
NM_001354810.1:c.1478T>C	NP_001341739.1:p.Ile493Thr
NR_148971.1:n.1882T>C
NM_001354809.2:c.1478T>C	NP_001341738.1:p.Ile493Thr
NM_001354810.2:c.1478T>C	NP_001341739.1:p.Ile493Thr
NR_148971.2:n.1901T>C
NM_000142.5:c.1475T>C MANE Select	NP_000133.1:p.Ile492Thr
NM_001163213.2:c.1481T>C	NP_001156685.1:p.Ile494Thr
NM_022965.4:c.1139T>C	NP_075254.1:p.Ile380Thr