Canonical Allele Identifier: CA608987817

Gene: FLT3

Linked Data

• dbSNP Id: rs1483580603
• gnomAD v2: 13-28608349-T-TAAGGGCGAATTCTGCAGATATCCATCACACTGGCGGCCGCTCGAGCA
• MyVariant Identifiers: chr13:g.28608349_28608350insAAGGGCGAATTCTGCAGATATCCATCACACTGGCGGCCGCTCGAGCA (hg19) ; chr13:g.28034212_28034213insAAGGGCGAATTCTGCAGATATCCATCACACTGGCGGCCGCTCGAGCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034212_28034213insAAGGGCGAATTCTGCAGATATCCATCACACTGGCGGCCGCTCGAGCA , CM000675.2:g.28034212_28034213insAAGGGCGAATTCTGCAGATATCCATCACACTGGCGGCCGCTCGAGCA	GRCh38
NC_000013.10:g.28608349_28608350insAAGGGCGAATTCTGCAGATATCCATCACACTGGCGGCCGCTCGAGCA , CM000675.1:g.28608349_28608350insAAGGGCGAATTCTGCAGATATCCATCACACTGGCGGCCGCTCGAGCA	GRCh37
NC_000013.9:g.27506349_27506350insAAGGGCGAATTCTGCAGATATCCATCACACTGGCGGCCGCTCGAGCA	NCBI36
NG_007066.1:g.71356_71357insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT , LRG_457:g.71356_71357insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1706_1707insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT MANE Select	ENSP00000241453.7:p.Gln569HisfsTer29
ENST00000241453.11:c.1706_1707insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT	ENSP00000241453.7:p.Gln569HisfsTer29
ENST00000380987.2:c.1706_1707insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT	ENSP00000370374.2:p.Gln569HisfsTer29
NM_004119.2:c.1706_1707insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT , LRG_457t1:c.1706_1707insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT	NP_004110.2:p.Gln569HisfsTer29
NR_130706.1:n.1788_1789insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT
XM_011535015.1:c.1649_1650insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT	XP_011533317.1:p.Gln550HisfsTer29
XM_011535016.1:c.1181_1182insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT	XP_011533318.1:p.Gln394HisfsTer29
XM_011535017.1:c.1181_1182insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT	XP_011533319.1:p.Gln394HisfsTer29
XM_011535018.1:c.1181_1182insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT	XP_011533320.1:p.Gln394HisfsTer29
XM_011535015.2:c.1649_1650insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT	XP_011533317.1:p.Gln550HisfsTer29
XM_011535017.2:c.1181_1182insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT	XP_011533319.1:p.Gln394HisfsTer29
XM_011535018.2:c.1181_1182insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT	XP_011533320.1:p.Gln394HisfsTer29
XM_017020486.1:c.1490_1491insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT	XP_016875975.1:p.Gln497HisfsTer29
XM_017020487.1:c.1181_1182insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT	XP_016875976.1:p.Gln394HisfsTer29
XM_017020488.1:c.827_828insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT	XP_016875977.1:p.Gln276HisfsTer29
XM_017020489.1:c.809_810insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT	XP_016875978.1:p.Gln270HisfsTer29
NM_004119.3:c.1706_1707insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT MANE Select	NP_004110.2:p.Gln569HisfsTer29
NR_130706.2:n.1772_1773insTGCTCGAGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTT