Canonical Allele Identifier: CA247288987

Gene: FLT3

Linked Data

• dbSNP Id: rs777429979
• gnomAD v3: 13-28017949-CCA-C
• gnomAD v4: 13-28017949-CCA-C
• MyVariant Identifiers: chr13:g.28592087_28592088del (hg19) ; chr13:g.28017950_28017951del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28017951_28017952del , CM000675.2:g.28017951_28017952del	GRCh38
NC_000013.10:g.28592088_28592089del , CM000675.1:g.28592088_28592089del	GRCh37
NC_000013.9:g.27490088_27490089del	NCBI36
NG_007066.1:g.87618_87619del , LRG_457:g.87618_87619del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2541+516_2541+517del MANE Select	ENSP00000241453.7:n.2541+516_2541+517del
ENST00000241453.11:c.2541+516_2541+517del	ENSP00000241453.7:n.2541+516_2541+517del
ENST00000380987.2:c.*453+516_*453+517del	ENSP00000370374.2:n.*453+516_*453+517del
NM_004119.2:c.2541+516_2541+517del , LRG_457t1:c.2541+516_2541+517del	NP_004110.2:n.2541+516_2541+517del
NR_130706.1:n.2755+516_2755+517del
XM_011535015.1:c.2484+516_2484+517del	XP_011533317.1:n.2484+516_2484+517del
XM_011535016.1:c.2016+516_2016+517del	XP_011533318.1:n.2016+516_2016+517del
XM_011535017.1:c.2016+516_2016+517del	XP_011533319.1:n.2016+516_2016+517del
XM_011535018.1:c.2016+516_2016+517del	XP_011533320.1:n.2016+516_2016+517del
XM_011535015.2:c.2484+516_2484+517del	XP_011533317.1:n.2484+516_2484+517del
XM_011535017.2:c.2016+516_2016+517del	XP_011533319.1:n.2016+516_2016+517del
XM_011535018.2:c.2016+516_2016+517del	XP_011533320.1:n.2016+516_2016+517del
XM_017020486.1:c.2325+516_2325+517del	XP_016875975.1:n.2325+516_2325+517del
XM_017020487.1:c.2016+516_2016+517del	XP_016875976.1:n.2016+516_2016+517del
XM_017020488.1:c.1662+516_1662+517del	XP_016875977.1:n.1662+516_1662+517del
XM_017020489.1:c.1644+516_1644+517del	XP_016875978.1:n.1644+516_1644+517del
NM_004119.3:c.2541+516_2541+517del MANE Select	NP_004110.2:n.2541+516_2541+517del
NR_130706.2:n.2739+516_2739+517del