Canonical Allele Identifier: CA387650151

Gene: FLT3

Linked Data

• dbSNP Id: rs1479603384
• gnomAD v2: 13-28592615-C-T
• gnomAD v3: 13-28018478-C-T
• gnomAD v4: 13-28018478-C-T
• MyVariant Identifiers: chr13:g.28592615C>T (hg19) ; chr13:g.28018478C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018478C>T , CM000675.2:g.28018478C>T	GRCh38
NC_000013.10:g.28592615C>T , CM000675.1:g.28592615C>T	GRCh37
NC_000013.9:g.27490615C>T	NCBI36
NG_007066.1:g.87091G>A , LRG_457:g.87091G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2530G>A MANE Select	ENSP00000241453.7:p.Val844Ile
ENST00000241453.11:c.2530G>A	ENSP00000241453.7:p.Val844Ile
ENST00000380987.2:c.*442G>A	ENSP00000370374.2:n.*442G>A
NM_004119.2:c.2530G>A , LRG_457t1:c.2530G>A	NP_004110.2:p.Val844Ile
NR_130706.1:n.2744G>A
XM_011535015.1:c.2473G>A	XP_011533317.1:p.Val825Ile
XM_011535016.1:c.2005G>A	XP_011533318.1:p.Val669Ile
XM_011535017.1:c.2005G>A	XP_011533319.1:p.Val669Ile
XM_011535018.1:c.2005G>A	XP_011533320.1:p.Val669Ile
XM_011535015.2:c.2473G>A	XP_011533317.1:p.Val825Ile
XM_011535017.2:c.2005G>A	XP_011533319.1:p.Val669Ile
XM_011535018.2:c.2005G>A	XP_011533320.1:p.Val669Ile
XM_017020486.1:c.2314G>A	XP_016875975.1:p.Val772Ile
XM_017020487.1:c.2005G>A	XP_016875976.1:p.Val669Ile
XM_017020488.1:c.1651G>A	XP_016875977.1:p.Val551Ile
XM_017020489.1:c.1633G>A	XP_016875978.1:p.Val545Ile
NM_004119.3:c.2530G>A MANE Select	NP_004110.2:p.Val844Ile
NR_130706.2:n.2728G>A