Canonical Allele Identifier: CA696996694

Gene: FLT3

Linked Data

• dbSNP Id: rs35884842
• gnomAD v3: 13-28028089-AAGAGAGAGAG-A
• gnomAD v4: 13-28028089-AAGAGAGAGAG-A
• MyVariant Identifiers: chr13:g.28602227_28602236del (hg19) ; chr13:g.28028090_28028099del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028102_28028111del , CM000675.2:g.28028102_28028111del	GRCh38
NC_000013.10:g.28602239_28602248del , CM000675.1:g.28602239_28602248del	GRCh37
NC_000013.9:g.27500239_27500248del	NCBI36
NG_007066.1:g.77470_77479del , LRG_457:g.77470_77479del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2053+79_2053+88del MANE Select	ENSP00000241453.7:n.2053+79_2053+88del
ENST00000241453.11:c.2053+79_2053+88del	ENSP00000241453.7:n.2053+79_2053+88del
ENST00000380987.2:c.2053+79_2053+88del	ENSP00000370374.2:n.2053+79_2053+88del
NM_004119.2:c.2053+79_2053+88del , LRG_457t1:c.2053+79_2053+88del	NP_004110.2:n.2053+79_2053+88del
NR_130706.1:n.2135+79_2135+88del
XM_011535015.1:c.1996+79_1996+88del	XP_011533317.1:n.1996+79_1996+88del
XM_011535016.1:c.1528+79_1528+88del	XP_011533318.1:n.1528+79_1528+88del
XM_011535017.1:c.1528+79_1528+88del	XP_011533319.1:n.1528+79_1528+88del
XM_011535018.1:c.1528+79_1528+88del	XP_011533320.1:n.1528+79_1528+88del
XM_011535015.2:c.1996+79_1996+88del	XP_011533317.1:n.1996+79_1996+88del
XM_011535017.2:c.1528+79_1528+88del	XP_011533319.1:n.1528+79_1528+88del
XM_011535018.2:c.1528+79_1528+88del	XP_011533320.1:n.1528+79_1528+88del
XM_017020486.1:c.1837+79_1837+88del	XP_016875975.1:n.1837+79_1837+88del
XM_017020487.1:c.1528+79_1528+88del	XP_016875976.1:n.1528+79_1528+88del
XM_017020488.1:c.1174+79_1174+88del	XP_016875977.1:n.1174+79_1174+88del
XM_017020489.1:c.1156+79_1156+88del	XP_016875978.1:n.1156+79_1156+88del
NM_004119.3:c.2053+79_2053+88del MANE Select	NP_004110.2:n.2053+79_2053+88del
NR_130706.2:n.2119+79_2119+88del