Canonical Allele Identifier: CA387650152

Gene: FLT3

Linked Data

• MyVariant Identifiers: chr13:g.28592617A>C (hg19) ; chr13:g.28018480A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018480A>C , CM000675.2:g.28018480A>C	GRCh38
NC_000013.10:g.28592617A>C , CM000675.1:g.28592617A>C	GRCh37
NC_000013.9:g.27490617A>C	NCBI36
NG_007066.1:g.87089T>G , LRG_457:g.87089T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2528T>G MANE Select	ENSP00000241453.7:p.Val843Gly
ENST00000241453.11:c.2528T>G	ENSP00000241453.7:p.Val843Gly
ENST00000380987.2:c.*440T>G	ENSP00000370374.2:n.*440T>G
NM_004119.2:c.2528T>G , LRG_457t1:c.2528T>G	NP_004110.2:p.Val843Gly
NR_130706.1:n.2742T>G
XM_011535015.1:c.2471T>G	XP_011533317.1:p.Val824Gly
XM_011535016.1:c.2003T>G	XP_011533318.1:p.Val668Gly
XM_011535017.1:c.2003T>G	XP_011533319.1:p.Val668Gly
XM_011535018.1:c.2003T>G	XP_011533320.1:p.Val668Gly
XM_011535015.2:c.2471T>G	XP_011533317.1:p.Val824Gly
XM_011535017.2:c.2003T>G	XP_011533319.1:p.Val668Gly
XM_011535018.2:c.2003T>G	XP_011533320.1:p.Val668Gly
XM_017020486.1:c.2312T>G	XP_016875975.1:p.Val771Gly
XM_017020487.1:c.2003T>G	XP_016875976.1:p.Val668Gly
XM_017020488.1:c.1649T>G	XP_016875977.1:p.Val550Gly
XM_017020489.1:c.1631T>G	XP_016875978.1:p.Val544Gly
NM_004119.3:c.2528T>G MANE Select	NP_004110.2:p.Val843Gly
NR_130706.2:n.2726T>G