Canonical Allele Identifier: CA954395990

Gene: FLT3

Linked Data

• dbSNP Id: rs1872973773
• gnomAD v4: 13-28028102-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028103del , CM000675.2:g.28028103del	GRCh38
NC_000013.10:g.28602240del , CM000675.1:g.28602240del	GRCh37
NC_000013.9:g.27500240del	NCBI36
NG_007066.1:g.77466del , LRG_457:g.77466del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2053+75del MANE Select	ENSP00000241453.7:n.2053+75del
ENST00000241453.11:c.2053+75del	ENSP00000241453.7:n.2053+75del
ENST00000380987.2:c.2053+75del	ENSP00000370374.2:n.2053+75del
NM_004119.2:c.2053+75del , LRG_457t1:c.2053+75del	NP_004110.2:n.2053+75del
NR_130706.1:n.2135+75del
XM_011535015.1:c.1996+75del	XP_011533317.1:n.1996+75del
XM_011535016.1:c.1528+75del	XP_011533318.1:n.1528+75del
XM_011535017.1:c.1528+75del	XP_011533319.1:n.1528+75del
XM_011535018.1:c.1528+75del	XP_011533320.1:n.1528+75del
XM_011535015.2:c.1996+75del	XP_011533317.1:n.1996+75del
XM_011535017.2:c.1528+75del	XP_011533319.1:n.1528+75del
XM_011535018.2:c.1528+75del	XP_011533320.1:n.1528+75del
XM_017020486.1:c.1837+75del	XP_016875975.1:n.1837+75del
XM_017020487.1:c.1528+75del	XP_016875976.1:n.1528+75del
XM_017020488.1:c.1174+75del	XP_016875977.1:n.1174+75del
XM_017020489.1:c.1156+75del	XP_016875978.1:n.1156+75del
NM_004119.3:c.2053+75del MANE Select	NP_004110.2:n.2053+75del
NR_130706.2:n.2119+75del