Canonical Allele Identifier: CA2575379219

Gene: FLT3

Linked Data

• gnomAD v4: 13-28028110-AGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028111_28028112del , CM000675.2:g.28028111_28028112del	GRCh38
NC_000013.10:g.28602248_28602249del , CM000675.1:g.28602248_28602249del	GRCh37
NC_000013.9:g.27500248_27500249del	NCBI36
NG_007066.1:g.77457_77458del , LRG_457:g.77457_77458del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2053+66_2053+67del MANE Select	ENSP00000241453.7:n.2053+66_2053+67del
ENST00000241453.11:c.2053+66_2053+67del	ENSP00000241453.7:n.2053+66_2053+67del
ENST00000380987.2:c.2053+66_2053+67del	ENSP00000370374.2:n.2053+66_2053+67del
NM_004119.2:c.2053+66_2053+67del , LRG_457t1:c.2053+66_2053+67del	NP_004110.2:n.2053+66_2053+67del
NR_130706.1:n.2135+66_2135+67del
XM_011535015.1:c.1996+66_1996+67del	XP_011533317.1:n.1996+66_1996+67del
XM_011535016.1:c.1528+66_1528+67del	XP_011533318.1:n.1528+66_1528+67del
XM_011535017.1:c.1528+66_1528+67del	XP_011533319.1:n.1528+66_1528+67del
XM_011535018.1:c.1528+66_1528+67del	XP_011533320.1:n.1528+66_1528+67del
XM_011535015.2:c.1996+66_1996+67del	XP_011533317.1:n.1996+66_1996+67del
XM_011535017.2:c.1528+66_1528+67del	XP_011533319.1:n.1528+66_1528+67del
XM_011535018.2:c.1528+66_1528+67del	XP_011533320.1:n.1528+66_1528+67del
XM_017020486.1:c.1837+66_1837+67del	XP_016875975.1:n.1837+66_1837+67del
XM_017020487.1:c.1528+66_1528+67del	XP_016875976.1:n.1528+66_1528+67del
XM_017020488.1:c.1174+66_1174+67del	XP_016875977.1:n.1174+66_1174+67del
XM_017020489.1:c.1156+66_1156+67del	XP_016875978.1:n.1156+66_1156+67del
NM_004119.3:c.2053+66_2053+67del MANE Select	NP_004110.2:n.2053+66_2053+67del
NR_130706.2:n.2119+66_2119+67del