Canonical Allele Identifier: CA387650210

Gene: FLT3

Linked Data

• dbSNP Id: rs2137623259
• MyVariant Identifiers: chr13:g.28592648C>T (hg19) ; chr13:g.28018511C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018511C>T , CM000675.2:g.28018511C>T	GRCh38
NC_000013.10:g.28592648C>T , CM000675.1:g.28592648C>T	GRCh37
NC_000013.9:g.27490648C>T	NCBI36
NG_007066.1:g.87058G>A , LRG_457:g.87058G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2497G>A MANE Select	ENSP00000241453.7:p.Ala833Thr
ENST00000241453.11:c.2497G>A	ENSP00000241453.7:p.Ala833Thr
ENST00000380987.2:c.*409G>A	ENSP00000370374.2:n.*409G>A
NM_004119.2:c.2497G>A , LRG_457t1:c.2497G>A	NP_004110.2:p.Ala833Thr
NR_130706.1:n.2711G>A
XM_011535015.1:c.2440G>A	XP_011533317.1:p.Ala814Thr
XM_011535016.1:c.1972G>A	XP_011533318.1:p.Ala658Thr
XM_011535017.1:c.1972G>A	XP_011533319.1:p.Ala658Thr
XM_011535018.1:c.1972G>A	XP_011533320.1:p.Ala658Thr
XM_011535015.2:c.2440G>A	XP_011533317.1:p.Ala814Thr
XM_011535017.2:c.1972G>A	XP_011533319.1:p.Ala658Thr
XM_011535018.2:c.1972G>A	XP_011533320.1:p.Ala658Thr
XM_017020486.1:c.2281G>A	XP_016875975.1:p.Ala761Thr
XM_017020487.1:c.1972G>A	XP_016875976.1:p.Ala658Thr
XM_017020488.1:c.1618G>A	XP_016875977.1:p.Ala540Thr
XM_017020489.1:c.1600G>A	XP_016875978.1:p.Ala534Thr
NM_004119.3:c.2497G>A MANE Select	NP_004110.2:p.Ala833Thr
NR_130706.2:n.2695G>A