Canonical Allele Identifier: CA954395999

Gene: FLT3

Linked Data

• gnomAD v3: 13-28028108-AG-A
• gnomAD v4: 13-28028108-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028109del , CM000675.2:g.28028109del	GRCh38
NC_000013.10:g.28602246del , CM000675.1:g.28602246del	GRCh37
NC_000013.9:g.27500246del	NCBI36
NG_007066.1:g.77460del , LRG_457:g.77460del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2053+69del MANE Select	ENSP00000241453.7:n.2053+69del
ENST00000241453.11:c.2053+69del	ENSP00000241453.7:n.2053+69del
ENST00000380987.2:c.2053+69del	ENSP00000370374.2:n.2053+69del
NM_004119.2:c.2053+69del , LRG_457t1:c.2053+69del	NP_004110.2:n.2053+69del
NR_130706.1:n.2135+69del
XM_011535015.1:c.1996+69del	XP_011533317.1:n.1996+69del
XM_011535016.1:c.1528+69del	XP_011533318.1:n.1528+69del
XM_011535017.1:c.1528+69del	XP_011533319.1:n.1528+69del
XM_011535018.1:c.1528+69del	XP_011533320.1:n.1528+69del
XM_011535015.2:c.1996+69del	XP_011533317.1:n.1996+69del
XM_011535017.2:c.1528+69del	XP_011533319.1:n.1528+69del
XM_011535018.2:c.1528+69del	XP_011533320.1:n.1528+69del
XM_017020486.1:c.1837+69del	XP_016875975.1:n.1837+69del
XM_017020487.1:c.1528+69del	XP_016875976.1:n.1528+69del
XM_017020488.1:c.1174+69del	XP_016875977.1:n.1174+69del
XM_017020489.1:c.1156+69del	XP_016875978.1:n.1156+69del
NM_004119.3:c.2053+69del MANE Select	NP_004110.2:n.2053+69del
NR_130706.2:n.2119+69del