Canonical Allele Identifier: CA387650221

Gene: FLT3

Linked Data

• dbSNP Id: rs1872093296
• MyVariant Identifiers: chr13:g.28592654C>A (hg19) ; chr13:g.28018517C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018517C>A , CM000675.2:g.28018517C>A	GRCh38
NC_000013.10:g.28592654C>A , CM000675.1:g.28592654C>A	GRCh37
NC_000013.9:g.27490654C>A	NCBI36
NG_007066.1:g.87052G>T , LRG_457:g.87052G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2491G>T MANE Select	ENSP00000241453.7:p.Gly831Ter
ENST00000241453.11:c.2491G>T	ENSP00000241453.7:p.Gly831Ter
ENST00000380987.2:c.*403G>T	ENSP00000370374.2:n.*403G>T
NM_004119.2:c.2491G>T , LRG_457t1:c.2491G>T	NP_004110.2:p.Gly831Ter
NR_130706.1:n.2705G>T
XM_011535015.1:c.2434G>T	XP_011533317.1:p.Gly812Ter
XM_011535016.1:c.1966G>T	XP_011533318.1:p.Gly656Ter
XM_011535017.1:c.1966G>T	XP_011533319.1:p.Gly656Ter
XM_011535018.1:c.1966G>T	XP_011533320.1:p.Gly656Ter
XM_011535015.2:c.2434G>T	XP_011533317.1:p.Gly812Ter
XM_011535017.2:c.1966G>T	XP_011533319.1:p.Gly656Ter
XM_011535018.2:c.1966G>T	XP_011533320.1:p.Gly656Ter
XM_017020486.1:c.2275G>T	XP_016875975.1:p.Gly759Ter
XM_017020487.1:c.1966G>T	XP_016875976.1:p.Gly656Ter
XM_017020488.1:c.1612G>T	XP_016875977.1:p.Gly538Ter
XM_017020489.1:c.1594G>T	XP_016875978.1:p.Gly532Ter
NM_004119.3:c.2491G>T MANE Select	NP_004110.2:p.Gly831Ter
NR_130706.2:n.2689G>T