Canonical Allele Identifier: CA387650351

Gene: FLT3

Linked Data

• dbSNP Id: rs2137624172
• gnomAD v4: 13-28018578-T-A
• MyVariant Identifiers: chr13:g.28592715T>A (hg19) ; chr13:g.28018578T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018578T>A , CM000675.2:g.28018578T>A	GRCh38
NC_000013.10:g.28592715T>A , CM000675.1:g.28592715T>A	GRCh37
NC_000013.9:g.27490715T>A	NCBI36
NG_007066.1:g.86991A>T , LRG_457:g.86991A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2430A>T MANE Select	ENSP00000241453.7:p.Arg810Ser
ENST00000241453.11:c.2430A>T	ENSP00000241453.7:p.Arg810Ser
ENST00000380987.2:c.*342A>T	ENSP00000370374.2:n.*342A>T
NM_004119.2:c.2430A>T , LRG_457t1:c.2430A>T	NP_004110.2:p.Arg810Ser
NR_130706.1:n.2644A>T
XM_011535015.1:c.2373A>T	XP_011533317.1:p.Arg791Ser
XM_011535016.1:c.1905A>T	XP_011533318.1:p.Arg635Ser
XM_011535017.1:c.1905A>T	XP_011533319.1:p.Arg635Ser
XM_011535018.1:c.1905A>T	XP_011533320.1:p.Arg635Ser
XM_011535015.2:c.2373A>T	XP_011533317.1:p.Arg791Ser
XM_011535017.2:c.1905A>T	XP_011533319.1:p.Arg635Ser
XM_011535018.2:c.1905A>T	XP_011533320.1:p.Arg635Ser
XM_017020486.1:c.2214A>T	XP_016875975.1:p.Arg738Ser
XM_017020487.1:c.1905A>T	XP_016875976.1:p.Arg635Ser
XM_017020488.1:c.1551A>T	XP_016875977.1:p.Arg517Ser
XM_017020489.1:c.1533A>T	XP_016875978.1:p.Arg511Ser
NM_004119.3:c.2430A>T MANE Select	NP_004110.2:p.Arg810Ser
NR_130706.2:n.2628A>T