Canonical Allele Identifier: CA608750509

Gene: FLT3

Linked Data

• dbSNP Id: rs35884842
• gnomAD v2: 13-28602226-A-AAGAG
• gnomAD v3: 13-28028089-A-AAGAG
• gnomAD v4: 13-28028089-A-AAGAG
• MyVariant Identifiers: chr13:g.28602234_28602235insAGAG (hg19) ; chr13:g.28602226_28602227insAGAG (hg19) ; chr13:g.28028097_28028098insAGAG (hg38) ; chr13:g.28028089_28028090insAGAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028108_28028111dup , CM000675.2:g.28028108_28028111dup	GRCh38
NC_000013.10:g.28602245_28602248dup , CM000675.1:g.28602245_28602248dup	GRCh37
NC_000013.9:g.27500245_27500248dup	NCBI36
NG_007066.1:g.77476_77479dup , LRG_457:g.77476_77479dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2053+85_2053+88dup MANE Select	ENSP00000241453.7:n.2053+85_2053+88dup
ENST00000241453.11:c.2053+85_2053+88dup	ENSP00000241453.7:n.2053+85_2053+88dup
ENST00000380987.2:c.2053+85_2053+88dup	ENSP00000370374.2:n.2053+85_2053+88dup
NM_004119.2:c.2053+85_2053+88dup , LRG_457t1:c.2053+85_2053+88dup	NP_004110.2:n.2053+85_2053+88dup
NR_130706.1:n.2135+85_2135+88dup
XM_011535015.1:c.1996+85_1996+88dup	XP_011533317.1:n.1996+85_1996+88dup
XM_011535016.1:c.1528+85_1528+88dup	XP_011533318.1:n.1528+85_1528+88dup
XM_011535017.1:c.1528+85_1528+88dup	XP_011533319.1:n.1528+85_1528+88dup
XM_011535018.1:c.1528+85_1528+88dup	XP_011533320.1:n.1528+85_1528+88dup
XM_011535015.2:c.1996+85_1996+88dup	XP_011533317.1:n.1996+85_1996+88dup
XM_011535017.2:c.1528+85_1528+88dup	XP_011533319.1:n.1528+85_1528+88dup
XM_011535018.2:c.1528+85_1528+88dup	XP_011533320.1:n.1528+85_1528+88dup
XM_017020486.1:c.1837+85_1837+88dup	XP_016875975.1:n.1837+85_1837+88dup
XM_017020487.1:c.1528+85_1528+88dup	XP_016875976.1:n.1528+85_1528+88dup
XM_017020488.1:c.1174+85_1174+88dup	XP_016875977.1:n.1174+85_1174+88dup
XM_017020489.1:c.1156+85_1156+88dup	XP_016875978.1:n.1156+85_1156+88dup
NM_004119.3:c.2053+85_2053+88dup MANE Select	NP_004110.2:n.2053+85_2053+88dup
NR_130706.2:n.2119+85_2119+88dup