Canonical Allele Identifier: CA6928308

Gene: FLT3

Linked Data

• dbSNP Id: rs769394501
• ExAC: 13:28592675 C / T
• gnomAD v2: 13-28592675-C-T
• gnomAD v3: 13-28018538-C-T
• gnomAD v4: 13-28018538-C-T
• MyVariant Identifiers: chr13:g.28592675C>T (hg19) ; chr13:g.28018538C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018538C>T , CM000675.2:g.28018538C>T	GRCh38
NC_000013.10:g.28592675C>T , CM000675.1:g.28592675C>T	GRCh37
NC_000013.9:g.27490675C>T	NCBI36
NG_007066.1:g.87031G>A , LRG_457:g.87031G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2470G>A MANE Select	ENSP00000241453.7:p.Val824Met
ENST00000241453.11:c.2470G>A	ENSP00000241453.7:p.Val824Met
ENST00000380987.2:c.*382G>A	ENSP00000370374.2:n.*382G>A
NM_004119.2:c.2470G>A , LRG_457t1:c.2470G>A	NP_004110.2:p.Val824Met
NR_130706.1:n.2684G>A
XM_011535015.1:c.2413G>A	XP_011533317.1:p.Val805Met
XM_011535016.1:c.1945G>A	XP_011533318.1:p.Val649Met
XM_011535017.1:c.1945G>A	XP_011533319.1:p.Val649Met
XM_011535018.1:c.1945G>A	XP_011533320.1:p.Val649Met
XM_011535015.2:c.2413G>A	XP_011533317.1:p.Val805Met
XM_011535017.2:c.1945G>A	XP_011533319.1:p.Val649Met
XM_011535018.2:c.1945G>A	XP_011533320.1:p.Val649Met
XM_017020486.1:c.2254G>A	XP_016875975.1:p.Val752Met
XM_017020487.1:c.1945G>A	XP_016875976.1:p.Val649Met
XM_017020488.1:c.1591G>A	XP_016875977.1:p.Val531Met
XM_017020489.1:c.1573G>A	XP_016875978.1:p.Val525Met
NM_004119.3:c.2470G>A MANE Select	NP_004110.2:p.Val824Met
NR_130706.2:n.2668G>A