Canonical Allele Identifier: CA483042221

Gene: FLT3

Linked Data

• MyVariant Identifiers: chr13:g.28592612T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018475T>G , CM000675.2:g.28018475T>G	GRCh38
NC_000013.10:g.28592612T>G , CM000675.1:g.28592612T>G	GRCh37
NC_000013.9:g.27490612T>G	NCBI36
NG_007066.1:g.87094A>C , LRG_457:g.87094A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2533A>C MANE Select	ENSP00000241453.7:p.Arg845=
ENST00000241453.11:c.2533A>C	ENSP00000241453.7:p.Arg845=
ENST00000380987.2:c.*445A>C	ENSP00000370374.2:n.*445A>C
NM_004119.2:c.2533A>C , LRG_457t1:c.2533A>C	NP_004110.2:p.Arg845=
NR_130706.1:n.2747A>C
XM_011535015.1:c.2476A>C	XP_011533317.1:p.Arg826=
XM_011535016.1:c.2008A>C	XP_011533318.1:p.Arg670=
XM_011535017.1:c.2008A>C	XP_011533319.1:p.Arg670=
XM_011535018.1:c.2008A>C	XP_011533320.1:p.Arg670=
XM_011535015.2:c.2476A>C	XP_011533317.1:p.Arg826=
XM_011535017.2:c.2008A>C	XP_011533319.1:p.Arg670=
XM_011535018.2:c.2008A>C	XP_011533320.1:p.Arg670=
XM_017020486.1:c.2317A>C	XP_016875975.1:p.Arg773=
XM_017020487.1:c.2008A>C	XP_016875976.1:p.Arg670=
XM_017020488.1:c.1654A>C	XP_016875977.1:p.Arg552=
XM_017020489.1:c.1636A>C	XP_016875978.1:p.Arg546=
NM_004119.3:c.2533A>C MANE Select	NP_004110.2:p.Arg845=
NR_130706.2:n.2731A>C