Canonical Allele Identifier: CA387640944

Gene: FLT3

Linked Data

• dbSNP Id: rs761757421
• gnomAD v4: 13-28034171-C-T
• MyVariant Identifiers: chr13:g.28608308C>T (hg19) ; chr13:g.28034171C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034171C>T , CM000675.2:g.28034171C>T	GRCh38
NC_000013.10:g.28608308C>T , CM000675.1:g.28608308C>T	GRCh37
NC_000013.9:g.27506308C>T	NCBI36
NG_007066.1:g.71398G>A , LRG_457:g.71398G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1748G>A MANE Select	ENSP00000241453.7:p.Gly583Asp
ENST00000241453.11:c.1748G>A	ENSP00000241453.7:p.Gly583Asp
ENST00000380987.2:c.1748G>A	ENSP00000370374.2:p.Gly583Asp
NM_004119.2:c.1748G>A , LRG_457t1:c.1748G>A	NP_004110.2:p.Gly583Asp
NR_130706.1:n.1830G>A
XM_011535015.1:c.1691G>A	XP_011533317.1:p.Gly564Asp
XM_011535016.1:c.1223G>A	XP_011533318.1:p.Gly408Asp
XM_011535017.1:c.1223G>A	XP_011533319.1:p.Gly408Asp
XM_011535018.1:c.1223G>A	XP_011533320.1:p.Gly408Asp
XM_011535015.2:c.1691G>A	XP_011533317.1:p.Gly564Asp
XM_011535017.2:c.1223G>A	XP_011533319.1:p.Gly408Asp
XM_011535018.2:c.1223G>A	XP_011533320.1:p.Gly408Asp
XM_017020486.1:c.1532G>A	XP_016875975.1:p.Gly511Asp
XM_017020487.1:c.1223G>A	XP_016875976.1:p.Gly408Asp
XM_017020488.1:c.869G>A	XP_016875977.1:p.Gly290Asp
XM_017020489.1:c.851G>A	XP_016875978.1:p.Gly284Asp
NM_004119.3:c.1748G>A MANE Select	NP_004110.2:p.Gly583Asp
NR_130706.2:n.1814G>A