Canonical Allele Identifier: CA387641014

Gene: FLT3

Linked Data

• dbSNP Id: rs2137675896
• MyVariant Identifiers: chr13:g.28608322C>G (hg19) ; chr13:g.28034185C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034185C>G , CM000675.2:g.28034185C>G	GRCh38
NC_000013.10:g.28608322C>G , CM000675.1:g.28608322C>G	GRCh37
NC_000013.9:g.27506322C>G	NCBI36
NG_007066.1:g.71384G>C , LRG_457:g.71384G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1734G>C MANE Select	ENSP00000241453.7:p.Met578Ile
ENST00000241453.11:c.1734G>C	ENSP00000241453.7:p.Met578Ile
ENST00000380987.2:c.1734G>C	ENSP00000370374.2:p.Met578Ile
NM_004119.2:c.1734G>C , LRG_457t1:c.1734G>C	NP_004110.2:p.Met578Ile
NR_130706.1:n.1816G>C
XM_011535015.1:c.1677G>C	XP_011533317.1:p.Met559Ile
XM_011535016.1:c.1209G>C	XP_011533318.1:p.Met403Ile
XM_011535017.1:c.1209G>C	XP_011533319.1:p.Met403Ile
XM_011535018.1:c.1209G>C	XP_011533320.1:p.Met403Ile
XM_011535015.2:c.1677G>C	XP_011533317.1:p.Met559Ile
XM_011535017.2:c.1209G>C	XP_011533319.1:p.Met403Ile
XM_011535018.2:c.1209G>C	XP_011533320.1:p.Met403Ile
XM_017020486.1:c.1518G>C	XP_016875975.1:p.Met506Ile
XM_017020487.1:c.1209G>C	XP_016875976.1:p.Met403Ile
XM_017020488.1:c.855G>C	XP_016875977.1:p.Met285Ile
XM_017020489.1:c.837G>C	XP_016875978.1:p.Met279Ile
NM_004119.3:c.1734G>C MANE Select	NP_004110.2:p.Met578Ile
NR_130706.2:n.1800G>C