Canonical Allele Identifier: CA280205

Gene: FLT3

Linked Data

• ClinVar Variation Id: 16271
• ClinVar RCV Id: RCV000017659
• dbSNP Id: rs398122514
• COSMIC: COSM850
• MyVariant Identifiers: chr13:g.28592624_28592625insGGATCC (hg19) ; chr13:g.28018487_28018488insGGATCC (hg38)
• PubMed: PMID:12384447

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018490_28018491insTCCGGA , CM000675.2:g.28018490_28018491insTCCGGA	GRCh38
NC_000013.10:g.28592627_28592628insTCCGGA , CM000675.1:g.28592627_28592628insTCCGGA	GRCh37
NC_000013.9:g.27490627_27490628insTCCGGA	NCBI36
NG_007066.1:g.87081_87082insGGATCC , LRG_457:g.87081_87082insGGATCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2520_2521insGGATCC MANE Select	ENSP00000241453.7:p.Ser840_Asn841insGlySer
ENST00000241453.11:c.2520_2521insGGATCC	ENSP00000241453.7:p.Ser840_Asn841insGlySer
ENST00000380987.2:c.*432_*433insGGATCC	ENSP00000370374.2:n.*432_*433insGGATCC
NM_004119.2:c.2520_2521insGGATCC , LRG_457t1:c.2520_2521insGGATCC	NP_004110.2:p.Ser840_Asn841insGlySer
NR_130706.1:n.2734_2735insGGATCC
XM_011535015.1:c.2463_2464insGGATCC	XP_011533317.1:p.Ser821_Asn822insGlySer
XM_011535016.1:c.1995_1996insGGATCC	XP_011533318.1:p.Ser665_Asn666insGlySer
XM_011535017.1:c.1995_1996insGGATCC	XP_011533319.1:p.Ser665_Asn666insGlySer
XM_011535018.1:c.1995_1996insGGATCC	XP_011533320.1:p.Ser665_Asn666insGlySer
XM_011535015.2:c.2463_2464insGGATCC	XP_011533317.1:p.Ser821_Asn822insGlySer
XM_011535017.2:c.1995_1996insGGATCC	XP_011533319.1:p.Ser665_Asn666insGlySer
XM_011535018.2:c.1995_1996insGGATCC	XP_011533320.1:p.Ser665_Asn666insGlySer
XM_017020486.1:c.2304_2305insGGATCC	XP_016875975.1:p.Ser768_Asn769insGlySer
XM_017020487.1:c.1995_1996insGGATCC	XP_016875976.1:p.Ser665_Asn666insGlySer
XM_017020488.1:c.1641_1642insGGATCC	XP_016875977.1:p.Ser547_Asn548insGlySer
XM_017020489.1:c.1623_1624insGGATCC	XP_016875978.1:p.Ser541_Asn542insGlySer
NM_004119.3:c.2520_2521insGGATCC MANE Select	NP_004110.2:p.Ser840_Asn841insGlySer
NR_130706.2:n.2718_2719insGGATCC