Canonical Allele Identifier: CA387650268

Gene: FLT3

Linked Data

• dbSNP Id: rs1221240514
• gnomAD v2: 13-28592674-A-G
• gnomAD v4: 13-28018537-A-G
• MyVariant Identifiers: chr13:g.28592674A>G (hg19) ; chr13:g.28018537A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018537A>G , CM000675.2:g.28018537A>G	GRCh38
NC_000013.10:g.28592674A>G , CM000675.1:g.28592674A>G	GRCh37
NC_000013.9:g.27490674A>G	NCBI36
NG_007066.1:g.87032T>C , LRG_457:g.87032T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2471T>C MANE Select	ENSP00000241453.7:p.Val824Ala
ENST00000241453.11:c.2471T>C	ENSP00000241453.7:p.Val824Ala
ENST00000380987.2:c.*383T>C	ENSP00000370374.2:n.*383T>C
NM_004119.2:c.2471T>C , LRG_457t1:c.2471T>C	NP_004110.2:p.Val824Ala
NR_130706.1:n.2685T>C
XM_011535015.1:c.2414T>C	XP_011533317.1:p.Val805Ala
XM_011535016.1:c.1946T>C	XP_011533318.1:p.Val649Ala
XM_011535017.1:c.1946T>C	XP_011533319.1:p.Val649Ala
XM_011535018.1:c.1946T>C	XP_011533320.1:p.Val649Ala
XM_011535015.2:c.2414T>C	XP_011533317.1:p.Val805Ala
XM_011535017.2:c.1946T>C	XP_011533319.1:p.Val649Ala
XM_011535018.2:c.1946T>C	XP_011533320.1:p.Val649Ala
XM_017020486.1:c.2255T>C	XP_016875975.1:p.Val752Ala
XM_017020487.1:c.1946T>C	XP_016875976.1:p.Val649Ala
XM_017020488.1:c.1592T>C	XP_016875977.1:p.Val531Ala
XM_017020489.1:c.1574T>C	XP_016875978.1:p.Val525Ala
NM_004119.3:c.2471T>C MANE Select	NP_004110.2:p.Val824Ala
NR_130706.2:n.2669T>C