Canonical Allele Identifier: CA387652143

Gene: FLT3

Linked Data

• gnomAD v4: 13-28028211-T-C
• MyVariant Identifiers: chr13:g.28602348T>C (hg19) ; chr13:g.28028211T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028211T>C , CM000675.2:g.28028211T>C	GRCh38
NC_000013.10:g.28602348T>C , CM000675.1:g.28602348T>C	GRCh37
NC_000013.9:g.27500348T>C	NCBI36
NG_007066.1:g.77358A>G , LRG_457:g.77358A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2020A>G MANE Select	ENSP00000241453.7:p.Ile674Val
ENST00000241453.11:c.2020A>G	ENSP00000241453.7:p.Ile674Val
ENST00000380987.2:c.2020A>G	ENSP00000370374.2:p.Ile674Val
NM_004119.2:c.2020A>G , LRG_457t1:c.2020A>G	NP_004110.2:p.Ile674Val
NR_130706.1:n.2102A>G
XM_011535015.1:c.1963A>G	XP_011533317.1:p.Ile655Val
XM_011535016.1:c.1495A>G	XP_011533318.1:p.Ile499Val
XM_011535017.1:c.1495A>G	XP_011533319.1:p.Ile499Val
XM_011535018.1:c.1495A>G	XP_011533320.1:p.Ile499Val
XM_011535015.2:c.1963A>G	XP_011533317.1:p.Ile655Val
XM_011535017.2:c.1495A>G	XP_011533319.1:p.Ile499Val
XM_011535018.2:c.1495A>G	XP_011533320.1:p.Ile499Val
XM_017020486.1:c.1804A>G	XP_016875975.1:p.Ile602Val
XM_017020487.1:c.1495A>G	XP_016875976.1:p.Ile499Val
XM_017020488.1:c.1141A>G	XP_016875977.1:p.Ile381Val
XM_017020489.1:c.1123A>G	XP_016875978.1:p.Ile375Val
NM_004119.3:c.2020A>G MANE Select	NP_004110.2:p.Ile674Val
NR_130706.2:n.2086A>G