Canonical Allele Identifier: CA2080790570

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028143_28028157delinsTTTTTGATGAGGTGA , CM000675.2:g.28028143_28028157delinsTTTTTGATGAGGTGA	GRCh38
NC_000013.10:g.28602280_28602294delinsTTTTTGATGAGGTGA , CM000675.1:g.28602280_28602294delinsTTTTTGATGAGGTGA	GRCh37
NC_000013.9:g.27500280_27500294delinsTTTTTGATGAGGTGA	NCBI36
NG_007066.1:g.77412_77426delinsTCACCTCATCAAAAA , LRG_457:g.77412_77426delinsTCACCTCATCAAAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2053+21_2053+35delinsTCACCTCATCAAAAA MANE Select	ENSP00000241453.7:n.2053+21_2053+35delins...
ENST00000241453.11:c.2053+21_2053+35delinsTCACCTCATCAAAAA	ENSP00000241453.7:n.2053+21_2053+35delins...
ENST00000380987.2:c.2053+21_2053+35delinsTCACCTCATCAAAAA	ENSP00000370374.2:n.2053+21_2053+35delins...
NM_004119.2:c.2053+21_2053+35delinsTCACCTCATCAAAAA , LRG_457t1:c.2053+21_2053+35delinsTCACCTCATCAAAAA	NP_004110.2:n.2053+21_2053+35delinsTCACCT...
NR_130706.1:n.2135+21_2135+35delinsTCACCTCATCAAAAA
XM_011535015.1:c.1996+21_1996+35delinsTCACCTCATCAAAAA	XP_011533317.1:n.1996+21_1996+35delinsTCA...
XM_011535016.1:c.1528+21_1528+35delinsTCACCTCATCAAAAA	XP_011533318.1:n.1528+21_1528+35delinsTCA...
XM_011535017.1:c.1528+21_1528+35delinsTCACCTCATCAAAAA	XP_011533319.1:n.1528+21_1528+35delinsTCA...
XM_011535018.1:c.1528+21_1528+35delinsTCACCTCATCAAAAA	XP_011533320.1:n.1528+21_1528+35delinsTCA...
XM_011535015.2:c.1996+21_1996+35delinsTCACCTCATCAAAAA	XP_011533317.1:n.1996+21_1996+35delinsTCA...
XM_011535017.2:c.1528+21_1528+35delinsTCACCTCATCAAAAA	XP_011533319.1:n.1528+21_1528+35delinsTCA...
XM_011535018.2:c.1528+21_1528+35delinsTCACCTCATCAAAAA	XP_011533320.1:n.1528+21_1528+35delinsTCA...
XM_017020486.1:c.1837+21_1837+35delinsTCACCTCATCAAAAA	XP_016875975.1:n.1837+21_1837+35delinsTCA...
XM_017020487.1:c.1528+21_1528+35delinsTCACCTCATCAAAAA	XP_016875976.1:n.1528+21_1528+35delinsTCA...
XM_017020488.1:c.1174+21_1174+35delinsTCACCTCATCAAAAA	XP_016875977.1:n.1174+21_1174+35delinsTCA...
XM_017020489.1:c.1156+21_1156+35delinsTCACCTCATCAAAAA	XP_016875978.1:n.1156+21_1156+35delinsTCA...
NM_004119.3:c.2053+21_2053+35delinsTCACCTCATCAAAAA MANE Select	NP_004110.2:n.2053+21_2053+35delinsTCACCT...
NR_130706.2:n.2119+21_2119+35delinsTCACCTCATCAAAAA