Canonical Allele Identifier: CA3202185832
Community Standard Title: NM_004119.3(FLT3):c.2498C= (p.Ala833=)
Gene: FLT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018510G= , CM000675.2:g.28018510G= GRCh38
NC_000013.10:g.28592647G= , CM000675.1:g.28592647G= GRCh37
NC_000013.9:g.27490647G= NCBI36
NG_007066.1:g.87059C= , LRG_457:g.87059C=

Transcript Alleles

HGVS Amino-acid Change
NM_004119.3:c.2498C= MANE Select NP_004110.2:p.Ala833=
ENST00000241453.12:c.2498C= MANE Select ENSP00000241453.7:p.Ala833=
NM_004119.2:c.2498C= , LRG_457t1:c.2498C= NP_004110.2:p.Ala833=
NR_130706.1:n.2712C=
NR_130706.2:n.2696C=
ENST00000241453.11:c.2498C= ENSP00000241453.7:p.Ala833=
ENST00000380987.2:c.*410C= ENSP00000370374.2:n.*410C=
XM_011535015.1:c.2441C= XP_011533317.1:p.Ala814=
XM_011535015.2:c.2441C= XP_011533317.1:p.Ala814=
XM_011535016.1:c.1973C= XP_011533318.1:p.Ala658=
XM_011535017.1:c.1973C= XP_011533319.1:p.Ala658=
XM_011535017.2:c.1973C= XP_011533319.1:p.Ala658=
XM_011535018.1:c.1973C= XP_011533320.1:p.Ala658=
XM_011535018.2:c.1973C= XP_011533320.1:p.Ala658=
XM_017020486.1:c.2282C= XP_016875975.1:p.Ala761=
XM_017020487.1:c.1973C= XP_016875976.1:p.Ala658=
XM_017020488.1:c.1619C= XP_016875977.1:p.Ala540=
XM_017020489.1:c.1601C= XP_016875978.1:p.Ala534=