Canonical Allele Identifier: CA954392072

Gene: FLT3

Linked Data

• dbSNP Id: rs1872107993
• gnomAD v3: 13-28018647-ATCTT-A
• gnomAD v4: 13-28018647-ATCTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018652_28018655del , CM000675.2:g.28018652_28018655del	GRCh38
NC_000013.10:g.28592789_28592792del , CM000675.1:g.28592789_28592792del	GRCh37
NC_000013.9:g.27490789_27490792del	NCBI36
NG_007066.1:g.86918_86921del , LRG_457:g.86918_86921del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2419-62_2419-59del MANE Select	ENSP00000241453.7:n.2419-62_2419-59del
ENST00000241453.11:c.2419-62_2419-59del	ENSP00000241453.7:n.2419-62_2419-59del
ENST00000380987.2:c.*331-62_*331-59del	ENSP00000370374.2:n.*331-62_*331-59del
NM_004119.2:c.2419-62_2419-59del , LRG_457t1:c.2419-62_2419-59del	NP_004110.2:n.2419-62_2419-59del
NR_130706.1:n.2633-62_2633-59del
XM_011535015.1:c.2362-62_2362-59del	XP_011533317.1:n.2362-62_2362-59del
XM_011535016.1:c.1894-62_1894-59del	XP_011533318.1:n.1894-62_1894-59del
XM_011535017.1:c.1894-62_1894-59del	XP_011533319.1:n.1894-62_1894-59del
XM_011535018.1:c.1894-62_1894-59del	XP_011533320.1:n.1894-62_1894-59del
XM_011535015.2:c.2362-62_2362-59del	XP_011533317.1:n.2362-62_2362-59del
XM_011535017.2:c.1894-62_1894-59del	XP_011533319.1:n.1894-62_1894-59del
XM_011535018.2:c.1894-62_1894-59del	XP_011533320.1:n.1894-62_1894-59del
XM_017020486.1:c.2203-62_2203-59del	XP_016875975.1:n.2203-62_2203-59del
XM_017020487.1:c.1894-62_1894-59del	XP_016875976.1:n.1894-62_1894-59del
XM_017020488.1:c.1540-62_1540-59del	XP_016875977.1:n.1540-62_1540-59del
XM_017020489.1:c.1522-62_1522-59del	XP_016875978.1:n.1522-62_1522-59del
NM_004119.3:c.2419-62_2419-59del MANE Select	NP_004110.2:n.2419-62_2419-59del
NR_130706.2:n.2617-62_2617-59del