Canonical Allele Identifier: CA387650357

Gene: FLT3

Linked Data

• dbSNP Id: rs2137624206
• gnomAD v4: 13-28018580-T-C
• MyVariant Identifiers: chr13:g.28592717T>C (hg19) ; chr13:g.28018580T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018580T>C , CM000675.2:g.28018580T>C	GRCh38
NC_000013.10:g.28592717T>C , CM000675.1:g.28592717T>C	GRCh37
NC_000013.9:g.27490717T>C	NCBI36
NG_007066.1:g.86989A>G , LRG_457:g.86989A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2428A>G MANE Select	ENSP00000241453.7:p.Arg810Gly
ENST00000241453.11:c.2428A>G	ENSP00000241453.7:p.Arg810Gly
ENST00000380987.2:c.*340A>G	ENSP00000370374.2:n.*340A>G
NM_004119.2:c.2428A>G , LRG_457t1:c.2428A>G	NP_004110.2:p.Arg810Gly
NR_130706.1:n.2642A>G
XM_011535015.1:c.2371A>G	XP_011533317.1:p.Arg791Gly
XM_011535016.1:c.1903A>G	XP_011533318.1:p.Arg635Gly
XM_011535017.1:c.1903A>G	XP_011533319.1:p.Arg635Gly
XM_011535018.1:c.1903A>G	XP_011533320.1:p.Arg635Gly
XM_011535015.2:c.2371A>G	XP_011533317.1:p.Arg791Gly
XM_011535017.2:c.1903A>G	XP_011533319.1:p.Arg635Gly
XM_011535018.2:c.1903A>G	XP_011533320.1:p.Arg635Gly
XM_017020486.1:c.2212A>G	XP_016875975.1:p.Arg738Gly
XM_017020487.1:c.1903A>G	XP_016875976.1:p.Arg635Gly
XM_017020488.1:c.1549A>G	XP_016875977.1:p.Arg517Gly
XM_017020489.1:c.1531A>G	XP_016875978.1:p.Arg511Gly
NM_004119.3:c.2428A>G MANE Select	NP_004110.2:p.Arg810Gly
NR_130706.2:n.2626A>G