Canonical Allele Identifier: CA6928468

Gene: FLT3

Linked Data

• dbSNP Id: rs771093551
• ExAC: 13:28602279 CTT / C
• gnomAD v2: 13-28602279-CTT-C
• gnomAD v3: 13-28028142-CTT-C
• gnomAD v4: 13-28028142-CTT-C
• MyVariant Identifiers: chr13:g.28602280_28602281del (hg19) ; chr13:g.28028143_28028144del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028146_28028147del , CM000675.2:g.28028146_28028147del	GRCh38
NC_000013.10:g.28602283_28602284del , CM000675.1:g.28602283_28602284del	GRCh37
NC_000013.9:g.27500283_27500284del	NCBI36
NG_007066.1:g.77425_77426del , LRG_457:g.77425_77426del

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2053+34_2053+35del MANE Select	ENSP00000241453.7:n.2053+34_2053+35del
ENST00000241453.11:c.2053+34_2053+35del	ENSP00000241453.7:n.2053+34_2053+35del
ENST00000380987.2:c.2053+34_2053+35del	ENSP00000370374.2:n.2053+34_2053+35del
NM_004119.2:c.2053+34_2053+35del , LRG_457t1:c.2053+34_2053+35del	NP_004110.2:n.2053+34_2053+35del
NR_130706.1:n.2135+34_2135+35del
XM_011535015.1:c.1996+34_1996+35del	XP_011533317.1:n.1996+34_1996+35del
XM_011535016.1:c.1528+34_1528+35del	XP_011533318.1:n.1528+34_1528+35del
XM_011535017.1:c.1528+34_1528+35del	XP_011533319.1:n.1528+34_1528+35del
XM_011535018.1:c.1528+34_1528+35del	XP_011533320.1:n.1528+34_1528+35del
XM_011535015.2:c.1996+34_1996+35del	XP_011533317.1:n.1996+34_1996+35del
XM_011535017.2:c.1528+34_1528+35del	XP_011533319.1:n.1528+34_1528+35del
XM_011535018.2:c.1528+34_1528+35del	XP_011533320.1:n.1528+34_1528+35del
XM_017020486.1:c.1837+34_1837+35del	XP_016875975.1:n.1837+34_1837+35del
XM_017020487.1:c.1528+34_1528+35del	XP_016875976.1:n.1528+34_1528+35del
XM_017020488.1:c.1174+34_1174+35del	XP_016875977.1:n.1174+34_1174+35del
XM_017020489.1:c.1156+34_1156+35del	XP_016875978.1:n.1156+34_1156+35del
NM_004119.3:c.2053+34_2053+35del MANE Select	NP_004110.2:n.2053+34_2053+35del
NR_130706.2:n.2119+34_2119+35del