Canonical Allele Identifier: CA387650192

Gene: FLT3

Linked Data

• dbSNP Id: rs2137623000
• COSMIC: COSM5376584
• MyVariant Identifiers: chr13:g.28592634C>T (hg19) ; chr13:g.28018497C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018497C>T , CM000675.2:g.28018497C>T	GRCh38
NC_000013.10:g.28592634C>T , CM000675.1:g.28592634C>T	GRCh37
NC_000013.9:g.27490634C>T	NCBI36
NG_007066.1:g.87072G>A , LRG_457:g.87072G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2511G>A MANE Select	ENSP00000241453.7:p.Met837Ile
ENST00000241453.11:c.2511G>A	ENSP00000241453.7:p.Met837Ile
ENST00000380987.2:c.*423G>A	ENSP00000370374.2:n.*423G>A
NM_004119.2:c.2511G>A , LRG_457t1:c.2511G>A	NP_004110.2:p.Met837Ile
NR_130706.1:n.2725G>A
XM_011535015.1:c.2454G>A	XP_011533317.1:p.Met818Ile
XM_011535016.1:c.1986G>A	XP_011533318.1:p.Met662Ile
XM_011535017.1:c.1986G>A	XP_011533319.1:p.Met662Ile
XM_011535018.1:c.1986G>A	XP_011533320.1:p.Met662Ile
XM_011535015.2:c.2454G>A	XP_011533317.1:p.Met818Ile
XM_011535017.2:c.1986G>A	XP_011533319.1:p.Met662Ile
XM_011535018.2:c.1986G>A	XP_011533320.1:p.Met662Ile
XM_017020486.1:c.2295G>A	XP_016875975.1:p.Met765Ile
XM_017020487.1:c.1986G>A	XP_016875976.1:p.Met662Ile
XM_017020488.1:c.1632G>A	XP_016875977.1:p.Met544Ile
XM_017020489.1:c.1614G>A	XP_016875978.1:p.Met538Ile
NM_004119.3:c.2511G>A MANE Select	NP_004110.2:p.Met837Ile
NR_130706.2:n.2709G>A