Canonical Allele Identifier: CA2622472804

Gene: FLT3

Linked Data

• gnomAD v4: 13-28028145-T-TGA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028145_28028146insGA , CM000675.2:g.28028145_28028146insGA	GRCh38
NC_000013.10:g.28602282_28602283insGA , CM000675.1:g.28602282_28602283insGA	GRCh37
NC_000013.9:g.27500282_27500283insGA	NCBI36
NG_007066.1:g.77423_77424insTC , LRG_457:g.77423_77424insTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2053+32_2053+33insTC MANE Select	ENSP00000241453.7:n.2053+32_2053+33insTC
ENST00000241453.11:c.2053+32_2053+33insTC	ENSP00000241453.7:n.2053+32_2053+33insTC
ENST00000380987.2:c.2053+32_2053+33insTC	ENSP00000370374.2:n.2053+32_2053+33insTC
NM_004119.2:c.2053+32_2053+33insTC , LRG_457t1:c.2053+32_2053+33insTC	NP_004110.2:n.2053+32_2053+33insTC
NR_130706.1:n.2135+32_2135+33insTC
XM_011535015.1:c.1996+32_1996+33insTC	XP_011533317.1:n.1996+32_1996+33insTC
XM_011535016.1:c.1528+32_1528+33insTC	XP_011533318.1:n.1528+32_1528+33insTC
XM_011535017.1:c.1528+32_1528+33insTC	XP_011533319.1:n.1528+32_1528+33insTC
XM_011535018.1:c.1528+32_1528+33insTC	XP_011533320.1:n.1528+32_1528+33insTC
XM_011535015.2:c.1996+32_1996+33insTC	XP_011533317.1:n.1996+32_1996+33insTC
XM_011535017.2:c.1528+32_1528+33insTC	XP_011533319.1:n.1528+32_1528+33insTC
XM_011535018.2:c.1528+32_1528+33insTC	XP_011533320.1:n.1528+32_1528+33insTC
XM_017020486.1:c.1837+32_1837+33insTC	XP_016875975.1:n.1837+32_1837+33insTC
XM_017020487.1:c.1528+32_1528+33insTC	XP_016875976.1:n.1528+32_1528+33insTC
XM_017020488.1:c.1174+32_1174+33insTC	XP_016875977.1:n.1174+32_1174+33insTC
XM_017020489.1:c.1156+32_1156+33insTC	XP_016875978.1:n.1156+32_1156+33insTC
NM_004119.3:c.2053+32_2053+33insTC MANE Select	NP_004110.2:n.2053+32_2053+33insTC
NR_130706.2:n.2119+32_2119+33insTC