Canonical Allele Identifier: CA387650281

Gene: FLT3

Linked Data

• dbSNP Id: rs2137623637
• MyVariant Identifiers: chr13:g.28592680C>G (hg19) ; chr13:g.28018543C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018543C>G , CM000675.2:g.28018543C>G	GRCh38
NC_000013.10:g.28592680C>G , CM000675.1:g.28592680C>G	GRCh37
NC_000013.9:g.27490680C>G	NCBI36
NG_007066.1:g.87026G>C , LRG_457:g.87026G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2465G>C MANE Select	ENSP00000241453.7:p.Gly822Ala
ENST00000241453.11:c.2465G>C	ENSP00000241453.7:p.Gly822Ala
ENST00000380987.2:c.*377G>C	ENSP00000370374.2:n.*377G>C
NM_004119.2:c.2465G>C , LRG_457t1:c.2465G>C	NP_004110.2:p.Gly822Ala
NR_130706.1:n.2679G>C
XM_011535015.1:c.2408G>C	XP_011533317.1:p.Gly803Ala
XM_011535016.1:c.1940G>C	XP_011533318.1:p.Gly647Ala
XM_011535017.1:c.1940G>C	XP_011533319.1:p.Gly647Ala
XM_011535018.1:c.1940G>C	XP_011533320.1:p.Gly647Ala
XM_011535015.2:c.2408G>C	XP_011533317.1:p.Gly803Ala
XM_011535017.2:c.1940G>C	XP_011533319.1:p.Gly647Ala
XM_011535018.2:c.1940G>C	XP_011533320.1:p.Gly647Ala
XM_017020486.1:c.2249G>C	XP_016875975.1:p.Gly750Ala
XM_017020487.1:c.1940G>C	XP_016875976.1:p.Gly647Ala
XM_017020488.1:c.1586G>C	XP_016875977.1:p.Gly529Ala
XM_017020489.1:c.1568G>C	XP_016875978.1:p.Gly523Ala
NM_004119.3:c.2465G>C MANE Select	NP_004110.2:p.Gly822Ala
NR_130706.2:n.2663G>C