Canonical Allele Identifier: CA6928475

Gene: FLT3

Linked Data

• dbSNP Id: rs367795676
• ExAC: 13:28602293 G / T
• gnomAD v2: 13-28602293-G-T
• gnomAD v3: 13-28028156-G-T
• gnomAD v4: 13-28028156-G-T
• MyVariant Identifiers: chr13:g.28602293G>T (hg19) ; chr13:g.28028156G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028156G>T , CM000675.2:g.28028156G>T	GRCh38
NC_000013.10:g.28602293G>T , CM000675.1:g.28602293G>T	GRCh37
NC_000013.9:g.27500293G>T	NCBI36
NG_007066.1:g.77413C>A , LRG_457:g.77413C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2053+22C>A MANE Select	ENSP00000241453.7:n.2053+22C>A
ENST00000241453.11:c.2053+22C>A	ENSP00000241453.7:n.2053+22C>A
ENST00000380987.2:c.2053+22C>A	ENSP00000370374.2:n.2053+22C>A
NM_004119.2:c.2053+22C>A , LRG_457t1:c.2053+22C>A	NP_004110.2:n.2053+22C>A
NR_130706.1:n.2135+22C>A
XM_011535015.1:c.1996+22C>A	XP_011533317.1:n.1996+22C>A
XM_011535016.1:c.1528+22C>A	XP_011533318.1:n.1528+22C>A
XM_011535017.1:c.1528+22C>A	XP_011533319.1:n.1528+22C>A
XM_011535018.1:c.1528+22C>A	XP_011533320.1:n.1528+22C>A
XM_011535015.2:c.1996+22C>A	XP_011533317.1:n.1996+22C>A
XM_011535017.2:c.1528+22C>A	XP_011533319.1:n.1528+22C>A
XM_011535018.2:c.1528+22C>A	XP_011533320.1:n.1528+22C>A
XM_017020486.1:c.1837+22C>A	XP_016875975.1:n.1837+22C>A
XM_017020487.1:c.1528+22C>A	XP_016875976.1:n.1528+22C>A
XM_017020488.1:c.1174+22C>A	XP_016875977.1:n.1174+22C>A
XM_017020489.1:c.1156+22C>A	XP_016875978.1:n.1156+22C>A
NM_004119.3:c.2053+22C>A MANE Select	NP_004110.2:n.2053+22C>A
NR_130706.2:n.2119+22C>A