Canonical Allele Identifier: CA2622472634

Gene: FLT3

Linked Data

• gnomAD v4: 13-28028052-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028052A>T , CM000675.2:g.28028052A>T	GRCh38
NC_000013.10:g.28602189A>T , CM000675.1:g.28602189A>T	GRCh37
NC_000013.9:g.27500189A>T	NCBI36
NG_007066.1:g.77517T>A , LRG_457:g.77517T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2053+126T>A MANE Select	ENSP00000241453.7:n.2053+126T>A
ENST00000241453.11:c.2053+126T>A	ENSP00000241453.7:n.2053+126T>A
ENST00000380987.2:c.2053+126T>A	ENSP00000370374.2:n.2053+126T>A
NM_004119.2:c.2053+126T>A , LRG_457t1:c.2053+126T>A	NP_004110.2:n.2053+126T>A
NR_130706.1:n.2135+126T>A
XM_011535015.1:c.1996+126T>A	XP_011533317.1:n.1996+126T>A
XM_011535016.1:c.1528+126T>A	XP_011533318.1:n.1528+126T>A
XM_011535017.1:c.1528+126T>A	XP_011533319.1:n.1528+126T>A
XM_011535018.1:c.1528+126T>A	XP_011533320.1:n.1528+126T>A
XM_011535015.2:c.1996+126T>A	XP_011533317.1:n.1996+126T>A
XM_011535017.2:c.1528+126T>A	XP_011533319.1:n.1528+126T>A
XM_011535018.2:c.1528+126T>A	XP_011533320.1:n.1528+126T>A
XM_017020486.1:c.1837+126T>A	XP_016875975.1:n.1837+126T>A
XM_017020487.1:c.1528+126T>A	XP_016875976.1:n.1528+126T>A
XM_017020488.1:c.1174+126T>A	XP_016875977.1:n.1174+126T>A
XM_017020489.1:c.1156+126T>A	XP_016875978.1:n.1156+126T>A
NM_004119.3:c.2053+126T>A MANE Select	NP_004110.2:n.2053+126T>A
NR_130706.2:n.2119+126T>A