Canonical Allele Identifier: CA2575379273
Gene: FLT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034232_28034234del , CM000675.2:g.28034232_28034234del GRCh38
NC_000013.10:g.28608369_28608371del , CM000675.1:g.28608369_28608371del GRCh37
NC_000013.9:g.27506369_27506371del NCBI36
NG_007066.1:g.71339_71341del , LRG_457:g.71339_71341del

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.1705-16_1705-14del MANE Select ENSP00000241453.7:n.1705-16_1705-14del
ENST00000241453.11:c.1705-16_1705-14del ENSP00000241453.7:n.1705-16_1705-14del
ENST00000380987.2:c.1705-16_1705-14del ENSP00000370374.2:n.1705-16_1705-14del
NM_004119.2:c.1705-16_1705-14del , LRG_457t1:c.1705-16_1705-14del NP_004110.2:n.1705-16_1705-14del
NR_130706.1:n.1787-16_1787-14del
XM_011535015.1:c.1648-16_1648-14del XP_011533317.1:n.1648-16_1648-14del
XM_011535016.1:c.1180-16_1180-14del XP_011533318.1:n.1180-16_1180-14del
XM_011535017.1:c.1180-16_1180-14del XP_011533319.1:n.1180-16_1180-14del
XM_011535018.1:c.1180-16_1180-14del XP_011533320.1:n.1180-16_1180-14del
XM_011535015.2:c.1648-16_1648-14del XP_011533317.1:n.1648-16_1648-14del
XM_011535017.2:c.1180-16_1180-14del XP_011533319.1:n.1180-16_1180-14del
XM_011535018.2:c.1180-16_1180-14del XP_011533320.1:n.1180-16_1180-14del
XM_017020486.1:c.1489-16_1489-14del XP_016875975.1:n.1489-16_1489-14del
XM_017020487.1:c.1180-16_1180-14del XP_016875976.1:n.1180-16_1180-14del
XM_017020488.1:c.826-16_826-14del XP_016875977.1:n.826-16_826-14del
XM_017020489.1:c.808-16_808-14del XP_016875978.1:n.808-16_808-14del
NM_004119.3:c.1705-16_1705-14del MANE Select NP_004110.2:n.1705-16_1705-14del
NR_130706.2:n.1771-16_1771-14del