Canonical Allele Identifier: CA2622473015
Gene: FLT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28028311A>T , CM000675.2:g.28028311A>T GRCh38
NC_000013.10:g.28602448A>T , CM000675.1:g.28602448A>T GRCh37
NC_000013.9:g.27500448A>T NCBI36
NG_007066.1:g.77258T>A , LRG_457:g.77258T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.1943-23T>A MANE Select ENSP00000241453.7:n.1943-23T>A
ENST00000241453.11:c.1943-23T>A ENSP00000241453.7:n.1943-23T>A
ENST00000380987.2:c.1943-23T>A ENSP00000370374.2:n.1943-23T>A
NM_004119.2:c.1943-23T>A , LRG_457t1:c.1943-23T>A NP_004110.2:n.1943-23T>A
NR_130706.1:n.2025-23T>A
XM_011535015.1:c.1886-23T>A XP_011533317.1:n.1886-23T>A
XM_011535016.1:c.1418-23T>A XP_011533318.1:n.1418-23T>A
XM_011535017.1:c.1418-23T>A XP_011533319.1:n.1418-23T>A
XM_011535018.1:c.1418-23T>A XP_011533320.1:n.1418-23T>A
XM_011535015.2:c.1886-23T>A XP_011533317.1:n.1886-23T>A
XM_011535017.2:c.1418-23T>A XP_011533319.1:n.1418-23T>A
XM_011535018.2:c.1418-23T>A XP_011533320.1:n.1418-23T>A
XM_017020486.1:c.1727-23T>A XP_016875975.1:n.1727-23T>A
XM_017020487.1:c.1418-23T>A XP_016875976.1:n.1418-23T>A
XM_017020488.1:c.1064-23T>A XP_016875977.1:n.1064-23T>A
XM_017020489.1:c.1046-23T>A XP_016875978.1:n.1046-23T>A
NM_004119.3:c.1943-23T>A MANE Select NP_004110.2:n.1943-23T>A
NR_130706.2:n.2009-23T>A