Canonical Allele Identifier: CA791737975

Gene: FGFR3

Linked Data

• dbSNP Id: rs1336375791
• MyVariant Identifiers: chr4:g.1806921_1806922del (hg19) ; chr4:g.1805194_1805195del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805196_1805197del , CM000666.2:g.1805196_1805197del	GRCh38
NC_000004.11:g.1806923_1806924del , CM000666.1:g.1806923_1806924del	GRCh37
NC_000004.10:g.1776721_1776722del	NCBI36
NG_012632.1:g.16885_16886del , LRG_1021:g.16885_16886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1419-159_1419-158del	ENSP00000339824.4:n.1419-159_1419-158del
ENST00000260795.8:c.*469-159_*469-158del	ENSP00000260795.3:n.*469-159_*469-158del
ENST00000352904.6:c.1077-159_1077-158del	ENSP00000231803.1:n.1077-159_1077-158del
ENST00000412135.7:c.1401-159_1401-158del	ENSP00000412903.3:n.1401-159_1401-158del
ENST00000440486.8:c.1413-159_1413-158del MANE Select	ENSP00000414914.2:n.1413-159_1413-158del
ENST00000481110.7:c.1416-159_1416-158del	ENSP00000420533.2:n.1416-159_1416-158del
ENST00000260795.6:c.1413-159_1413-158del	ENSP00000260795.2:n.1413-159_1413-158del
ENST00000340107.8:c.1419-159_1419-158del	ENSP00000339824.4:n.1419-159_1419-158del
ENST00000352904.5:c.1077-159_1077-158del	ENSP00000231803.1:n.1077-159_1077-158del
ENST00000412135.6:c.1077-159_1077-158del	ENSP00000412903.2:n.1077-159_1077-158del
ENST00000440486.6:c.1413-159_1413-158del	ENSP00000414914.2:n.1413-159_1413-158del
ENST00000469068.1:n.479-159_479-158del
ENST00000481110.6:c.1416-159_1416-158del	ENSP00000420533.2:n.1416-159_1416-158del
ENST00000613647.4:c.*469-159_*469-158del	ENSP00000479472.1:n.*469-159_*469-158del
NM_000142.4:c.1413-159_1413-158del , LRG_1021t1:c.1413-159_1413-158del	NP_000133.1:n.1413-159_1413-158del
NM_001163213.1:c.1419-159_1419-158del , LRG_1021t2:c.1419-159_1419-158del	NP_001156685.1:n.1419-159_1419-158del
NM_022965.3:c.1077-159_1077-158del	NP_075254.1:n.1077-159_1077-158del
XM_006713868.1:c.1425-159_1425-158del	XP_006713931.1:n.1425-159_1425-158del
XM_006713869.1:c.1425-159_1425-158del	XP_006713932.1:n.1425-159_1425-158del
XM_006713870.1:c.1422-159_1422-158del	XP_006713933.1:n.1422-159_1422-158del
XM_006713871.1:c.1419-159_1419-158del	XP_006713934.1:n.1419-159_1419-158del
XM_006713872.1:c.1416-159_1416-158del	XP_006713935.1:n.1416-159_1416-158del
XM_006713873.1:c.1413-159_1413-158del	XP_006713936.1:n.1413-159_1413-158del
XM_011513420.1:c.1419-159_1419-158del	XP_011511722.1:n.1419-159_1419-158del
XM_011513422.1:c.1416-159_1416-158del	XP_011511724.1:n.1416-159_1416-158del
NM_001354809.1:c.1416-159_1416-158del	NP_001341738.1:n.1416-159_1416-158del
NM_001354810.1:c.1416-159_1416-158del	NP_001341739.1:n.1416-159_1416-158del
NR_148971.1:n.1820-159_1820-158del
NM_001354809.2:c.1416-159_1416-158del	NP_001341738.1:n.1416-159_1416-158del
NM_001354810.2:c.1416-159_1416-158del	NP_001341739.1:n.1416-159_1416-158del
NR_148971.2:n.1839-159_1839-158del
NM_000142.5:c.1413-159_1413-158del MANE Select	NP_000133.1:n.1413-159_1413-158del
NM_001163213.2:c.1419-159_1419-158del	NP_001156685.1:n.1419-159_1419-158del
NM_022965.4:c.1077-159_1077-158del	NP_075254.1:n.1077-159_1077-158del