Canonical Allele Identifier: CA387650315

Gene: FLT3

Linked Data

• dbSNP Id: rs2137623900
• MyVariant Identifiers: chr13:g.28592698T>A (hg19) ; chr13:g.28018561T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018561T>A , CM000675.2:g.28018561T>A	GRCh38
NC_000013.10:g.28592698T>A , CM000675.1:g.28592698T>A	GRCh37
NC_000013.9:g.27490698T>A	NCBI36
NG_007066.1:g.87008A>T , LRG_457:g.87008A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2447A>T MANE Select	ENSP00000241453.7:p.Asn816Ile
ENST00000241453.11:c.2447A>T	ENSP00000241453.7:p.Asn816Ile
ENST00000380987.2:c.*359A>T	ENSP00000370374.2:n.*359A>T
NM_004119.2:c.2447A>T , LRG_457t1:c.2447A>T	NP_004110.2:p.Asn816Ile
NR_130706.1:n.2661A>T
XM_011535015.1:c.2390A>T	XP_011533317.1:p.Asn797Ile
XM_011535016.1:c.1922A>T	XP_011533318.1:p.Asn641Ile
XM_011535017.1:c.1922A>T	XP_011533319.1:p.Asn641Ile
XM_011535018.1:c.1922A>T	XP_011533320.1:p.Asn641Ile
XM_011535015.2:c.2390A>T	XP_011533317.1:p.Asn797Ile
XM_011535017.2:c.1922A>T	XP_011533319.1:p.Asn641Ile
XM_011535018.2:c.1922A>T	XP_011533320.1:p.Asn641Ile
XM_017020486.1:c.2231A>T	XP_016875975.1:p.Asn744Ile
XM_017020487.1:c.1922A>T	XP_016875976.1:p.Asn641Ile
XM_017020488.1:c.1568A>T	XP_016875977.1:p.Asn523Ile
XM_017020489.1:c.1550A>T	XP_016875978.1:p.Asn517Ile
NM_004119.3:c.2447A>T MANE Select	NP_004110.2:p.Asn816Ile
NR_130706.2:n.2645A>T