Canonical Allele Identifier: CA387650198

Gene: FLT3

Linked Data

• dbSNP Id: rs1057520023
• COSMIC: COSM5879386
• MyVariant Identifiers: chr13:g.28592638A>G (hg19) ; chr13:g.28018501A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018501A>G , CM000675.2:g.28018501A>G	GRCh38
NC_000013.10:g.28592638A>G , CM000675.1:g.28592638A>G	GRCh37
NC_000013.9:g.27490638A>G	NCBI36
NG_007066.1:g.87068T>C , LRG_457:g.87068T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2507T>C MANE Select	ENSP00000241453.7:p.Ile836Thr
ENST00000241453.11:c.2507T>C	ENSP00000241453.7:p.Ile836Thr
ENST00000380987.2:c.*419T>C	ENSP00000370374.2:n.*419T>C
NM_004119.2:c.2507T>C , LRG_457t1:c.2507T>C	NP_004110.2:p.Ile836Thr
NR_130706.1:n.2721T>C
XM_011535015.1:c.2450T>C	XP_011533317.1:p.Ile817Thr
XM_011535016.1:c.1982T>C	XP_011533318.1:p.Ile661Thr
XM_011535017.1:c.1982T>C	XP_011533319.1:p.Ile661Thr
XM_011535018.1:c.1982T>C	XP_011533320.1:p.Ile661Thr
XM_011535015.2:c.2450T>C	XP_011533317.1:p.Ile817Thr
XM_011535017.2:c.1982T>C	XP_011533319.1:p.Ile661Thr
XM_011535018.2:c.1982T>C	XP_011533320.1:p.Ile661Thr
XM_017020486.1:c.2291T>C	XP_016875975.1:p.Ile764Thr
XM_017020487.1:c.1982T>C	XP_016875976.1:p.Ile661Thr
XM_017020488.1:c.1628T>C	XP_016875977.1:p.Ile543Thr
XM_017020489.1:c.1610T>C	XP_016875978.1:p.Ile537Thr
NM_004119.3:c.2507T>C MANE Select	NP_004110.2:p.Ile836Thr
NR_130706.2:n.2705T>C