Canonical Allele Identifier: CA483042273

Gene: FLT3

Linked Data

• dbSNP Id: rs1269797866
• gnomAD v2: 13-28592691-A-C
• gnomAD v4: 13-28018554-A-C
• MyVariant Identifiers: chr13:g.28592691A>C (hg19) ; chr13:g.28018554A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018554A>C , CM000675.2:g.28018554A>C	GRCh38
NC_000013.10:g.28592691A>C , CM000675.1:g.28592691A>C	GRCh37
NC_000013.9:g.27490691A>C	NCBI36
NG_007066.1:g.87015T>G , LRG_457:g.87015T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2454T>G MANE Select	ENSP00000241453.7:p.Leu818=
ENST00000241453.11:c.2454T>G	ENSP00000241453.7:p.Leu818=
ENST00000380987.2:c.*366T>G	ENSP00000370374.2:n.*366T>G
NM_004119.2:c.2454T>G , LRG_457t1:c.2454T>G	NP_004110.2:p.Leu818=
NR_130706.1:n.2668T>G
XM_011535015.1:c.2397T>G	XP_011533317.1:p.Leu799=
XM_011535016.1:c.1929T>G	XP_011533318.1:p.Leu643=
XM_011535017.1:c.1929T>G	XP_011533319.1:p.Leu643=
XM_011535018.1:c.1929T>G	XP_011533320.1:p.Leu643=
XM_011535015.2:c.2397T>G	XP_011533317.1:p.Leu799=
XM_011535017.2:c.1929T>G	XP_011533319.1:p.Leu643=
XM_011535018.2:c.1929T>G	XP_011533320.1:p.Leu643=
XM_017020486.1:c.2238T>G	XP_016875975.1:p.Leu746=
XM_017020487.1:c.1929T>G	XP_016875976.1:p.Leu643=
XM_017020488.1:c.1575T>G	XP_016875977.1:p.Leu525=
XM_017020489.1:c.1557T>G	XP_016875978.1:p.Leu519=
NM_004119.3:c.2454T>G MANE Select	NP_004110.2:p.Leu818=
NR_130706.2:n.2652T>G