Canonical Allele Identifier: CA16603127

Gene: FLT3

Linked Data

• ClinVar Variation Id: 376717
• ClinVar RCV Id: RCV000444162
• dbSNP Id: rs1057520023
• COSMIC: COSM19843
• MyVariant Identifiers: chr13:g.28592638A>C (hg19) ; chr13:g.28018501A>C (hg38)
• PubMed: PMID:14737077

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2507T>G MANE Select	ENSP00000241453.7:p.Ile836Ser
ENST00000241453.11:c.2507T>G	ENSP00000241453.7:p.Ile836Ser
ENST00000380987.2:c.*419T>G	ENSP00000370374.2:n.*419T>G
NM_004119.2:c.2507T>G , LRG_457t1:c.2507T>G	NP_004110.2:p.Ile836Ser
NR_130706.1:n.2721T>G
XM_011535015.1:c.2450T>G	XP_011533317.1:p.Ile817Ser
XM_011535016.1:c.1982T>G	XP_011533318.1:p.Ile661Ser
XM_011535017.1:c.1982T>G	XP_011533319.1:p.Ile661Ser
XM_011535018.1:c.1982T>G	XP_011533320.1:p.Ile661Ser
XM_011535015.2:c.2450T>G	XP_011533317.1:p.Ile817Ser
XM_011535017.2:c.1982T>G	XP_011533319.1:p.Ile661Ser
XM_011535018.2:c.1982T>G	XP_011533320.1:p.Ile661Ser
XM_017020486.1:c.2291T>G	XP_016875975.1:p.Ile764Ser
XM_017020487.1:c.1982T>G	XP_016875976.1:p.Ile661Ser
XM_017020488.1:c.1628T>G	XP_016875977.1:p.Ile543Ser
XM_017020489.1:c.1610T>G	XP_016875978.1:p.Ile537Ser
NM_004119.3:c.2507T>G MANE Select	NP_004110.2:p.Ile836Ser
NR_130706.2:n.2705T>G