Canonical Allele Identifier: CA2622474499

Gene: FLT3

Linked Data

• gnomAD v4: 13-28018407-CATG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018410_28018412del , CM000675.2:g.28018410_28018412del	GRCh38
NC_000013.10:g.28592547_28592549del , CM000675.1:g.28592547_28592549del	GRCh37
NC_000013.9:g.27490547_27490549del	NCBI36
NG_007066.1:g.87159_87161del , LRG_457:g.87159_87161del

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2541+57_2541+59del MANE Select	ENSP00000241453.7:n.2541+57_2541+59del
ENST00000241453.11:c.2541+57_2541+59del	ENSP00000241453.7:n.2541+57_2541+59del
ENST00000380987.2:c.*453+57_*453+59del	ENSP00000370374.2:n.*453+57_*453+59del
NM_004119.2:c.2541+57_2541+59del , LRG_457t1:c.2541+57_2541+59del	NP_004110.2:n.2541+57_2541+59del
NR_130706.1:n.2755+57_2755+59del
XM_011535015.1:c.2484+57_2484+59del	XP_011533317.1:n.2484+57_2484+59del
XM_011535016.1:c.2016+57_2016+59del	XP_011533318.1:n.2016+57_2016+59del
XM_011535017.1:c.2016+57_2016+59del	XP_011533319.1:n.2016+57_2016+59del
XM_011535018.1:c.2016+57_2016+59del	XP_011533320.1:n.2016+57_2016+59del
XM_011535015.2:c.2484+57_2484+59del	XP_011533317.1:n.2484+57_2484+59del
XM_011535017.2:c.2016+57_2016+59del	XP_011533319.1:n.2016+57_2016+59del
XM_011535018.2:c.2016+57_2016+59del	XP_011533320.1:n.2016+57_2016+59del
XM_017020486.1:c.2325+57_2325+59del	XP_016875975.1:n.2325+57_2325+59del
XM_017020487.1:c.2016+57_2016+59del	XP_016875976.1:n.2016+57_2016+59del
XM_017020488.1:c.1662+57_1662+59del	XP_016875977.1:n.1662+57_1662+59del
XM_017020489.1:c.1644+57_1644+59del	XP_016875978.1:n.1644+57_1644+59del
NM_004119.3:c.2541+57_2541+59del MANE Select	NP_004110.2:n.2541+57_2541+59del
NR_130706.2:n.2739+57_2739+59del