Canonical Allele Identifier: CA387652254

Gene: FLT3

Linked Data

• MyVariant Identifiers: chr13:g.28602396G>C (hg19) ; chr13:g.28028259G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028259G>C , CM000675.2:g.28028259G>C	GRCh38
NC_000013.10:g.28602396G>C , CM000675.1:g.28602396G>C	GRCh37
NC_000013.9:g.27500396G>C	NCBI36
NG_007066.1:g.77310C>G , LRG_457:g.77310C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1972C>G MANE Select	ENSP00000241453.7:p.Leu658Val
ENST00000241453.11:c.1972C>G	ENSP00000241453.7:p.Leu658Val
ENST00000380987.2:c.1972C>G	ENSP00000370374.2:p.Leu658Val
NM_004119.2:c.1972C>G , LRG_457t1:c.1972C>G	NP_004110.2:p.Leu658Val
NR_130706.1:n.2054C>G
XM_011535015.1:c.1915C>G	XP_011533317.1:p.Leu639Val
XM_011535016.1:c.1447C>G	XP_011533318.1:p.Leu483Val
XM_011535017.1:c.1447C>G	XP_011533319.1:p.Leu483Val
XM_011535018.1:c.1447C>G	XP_011533320.1:p.Leu483Val
XM_011535015.2:c.1915C>G	XP_011533317.1:p.Leu639Val
XM_011535017.2:c.1447C>G	XP_011533319.1:p.Leu483Val
XM_011535018.2:c.1447C>G	XP_011533320.1:p.Leu483Val
XM_017020486.1:c.1756C>G	XP_016875975.1:p.Leu586Val
XM_017020487.1:c.1447C>G	XP_016875976.1:p.Leu483Val
XM_017020488.1:c.1093C>G	XP_016875977.1:p.Leu365Val
XM_017020489.1:c.1075C>G	XP_016875978.1:p.Leu359Val
NM_004119.3:c.1972C>G MANE Select	NP_004110.2:p.Leu658Val
NR_130706.2:n.2038C>G