Canonical Allele Identifier: CA1433506925

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804704_1804708delinsCTTCA , CM000666.2:g.1804704_1804708delinsCTTCA	GRCh38
NC_000004.11:g.1806431_1806435delinsCTTCA , CM000666.1:g.1806431_1806435delinsCTTCA	GRCh37
NC_000004.10:g.1776229_1776233delinsCTTCA	NCBI36
NG_012632.1:g.16393_16397delinsCTTCA , LRG_1021:g.16393_16397delinsCTTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1273-120_1273-116delinsCTTCA	ENSP00000339824.4:n.1273-120_1273-116delinsCTTCA
ENST00000260795.8:c.*323-120_*323-116delinsCTTCA	ENSP00000260795.3:n.*323-120_*323-116delinsCTTCA
ENST00000352904.6:c.931-120_931-116delinsCTTCA	ENSP00000231803.1:n.931-120_931-116delinsCTTCA
ENST00000412135.7:c.1255-120_1255-116delinsCTTCA	ENSP00000412903.3:n.1255-120_1255-116delinsCTTCA
ENST00000440486.8:c.1267-120_1267-116delinsCTTCA MANE Select	ENSP00000414914.2:n.1267-120_1267-116delinsCTTCA
ENST00000481110.7:c.1267-117_1267-113delinsCTTCA	ENSP00000420533.2:n.1267-117_1267-113delinsCTTCA
ENST00000260795.6:c.1267-120_1267-116delinsCTTCA	ENSP00000260795.2:n.1267-120_1267-116delinsCTTCA
ENST00000340107.8:c.1273-120_1273-116delinsCTTCA	ENSP00000339824.4:n.1273-120_1273-116delinsCTTCA
ENST00000352904.5:c.931-120_931-116delinsCTTCA	ENSP00000231803.1:n.931-120_931-116delinsCTTCA
ENST00000412135.6:c.931-120_931-116delinsCTTCA	ENSP00000412903.2:n.931-120_931-116delinsCTTCA
ENST00000440486.6:c.1267-120_1267-116delinsCTTCA	ENSP00000414914.2:n.1267-120_1267-116delinsCTTCA
ENST00000469068.1:n.213_217delinsCTTCA
ENST00000481110.6:c.1267-117_1267-113delinsCTTCA	ENSP00000420533.2:n.1267-117_1267-113delinsCTTCA
ENST00000613647.4:c.*323-120_*323-116delinsCTTCA	ENSP00000479472.1:n.*323-120_*323-116delinsCTTCA
NM_000142.4:c.1267-120_1267-116delinsCTTCA , LRG_1021t1:c.1267-120_1267-116delinsCTTCA	NP_000133.1:n.1267-120_1267-116delinsCTTCA
NM_001163213.1:c.1273-120_1273-116delinsCTTCA , LRG_1021t2:c.1273-120_1273-116delinsCTTCA	NP_001156685.1:n.1273-120_1273-116delinsCTTCA
NM_022965.3:c.931-120_931-116delinsCTTCA	NP_075254.1:n.931-120_931-116delinsCTTCA
XM_006713868.1:c.1279-120_1279-116delinsCTTCA	XP_006713931.1:n.1279-120_1279-116delinsCTTCA
XM_006713869.1:c.1279-120_1279-116delinsCTTCA	XP_006713932.1:n.1279-120_1279-116delinsCTTCA
XM_006713870.1:c.1273-117_1273-113delinsCTTCA	XP_006713933.1:n.1273-117_1273-113delinsCTTCA
XM_006713871.1:c.1273-120_1273-116delinsCTTCA	XP_006713934.1:n.1273-120_1273-116delinsCTTCA
XM_006713872.1:c.1267-117_1267-113delinsCTTCA	XP_006713935.1:n.1267-117_1267-113delinsCTTCA
XM_006713873.1:c.1267-120_1267-116delinsCTTCA	XP_006713936.1:n.1267-120_1267-116delinsCTTCA
XM_011513420.1:c.1273-120_1273-116delinsCTTCA	XP_011511722.1:n.1273-120_1273-116delinsCTTCA
XM_011513422.1:c.1267-117_1267-113delinsCTTCA	XP_011511724.1:n.1267-117_1267-113delinsCTTCA
NM_001354809.1:c.1267-117_1267-113delinsCTTCA	NP_001341738.1:n.1267-117_1267-113delinsCTTCA
NM_001354810.1:c.1267-117_1267-113delinsCTTCA	NP_001341739.1:n.1267-117_1267-113delinsCTTCA
NR_148971.1:n.1674-120_1674-116delinsCTTCA
NM_001354809.2:c.1267-117_1267-113delinsCTTCA	NP_001341738.1:n.1267-117_1267-113delinsCTTCA
NM_001354810.2:c.1267-117_1267-113delinsCTTCA	NP_001341739.1:n.1267-117_1267-113delinsCTTCA
NR_148971.2:n.1693-120_1693-116delinsCTTCA
NM_000142.5:c.1267-120_1267-116delinsCTTCA MANE Select	NP_000133.1:n.1267-120_1267-116delinsCTTCA
NM_001163213.2:c.1273-120_1273-116delinsCTTCA	NP_001156685.1:n.1273-120_1273-116delinsCTTCA
NM_022965.4:c.931-120_931-116delinsCTTCA	NP_075254.1:n.931-120_931-116delinsCTTCA