Canonical Allele Identifier: CA483043397

Gene: FLT3

Linked Data

• MyVariant Identifiers: chr13:g.28602382G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028245G>C , CM000675.2:g.28028245G>C	GRCh38
NC_000013.10:g.28602382G>C , CM000675.1:g.28602382G>C	GRCh37
NC_000013.9:g.27500382G>C	NCBI36
NG_007066.1:g.77324C>G , LRG_457:g.77324C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1986C>G MANE Select	ENSP00000241453.7:p.Leu662=
ENST00000241453.11:c.1986C>G	ENSP00000241453.7:p.Leu662=
ENST00000380987.2:c.1986C>G	ENSP00000370374.2:p.Leu662=
NM_004119.2:c.1986C>G , LRG_457t1:c.1986C>G	NP_004110.2:p.Leu662=
NR_130706.1:n.2068C>G
XM_011535015.1:c.1929C>G	XP_011533317.1:p.Leu643=
XM_011535016.1:c.1461C>G	XP_011533318.1:p.Leu487=
XM_011535017.1:c.1461C>G	XP_011533319.1:p.Leu487=
XM_011535018.1:c.1461C>G	XP_011533320.1:p.Leu487=
XM_011535015.2:c.1929C>G	XP_011533317.1:p.Leu643=
XM_011535017.2:c.1461C>G	XP_011533319.1:p.Leu487=
XM_011535018.2:c.1461C>G	XP_011533320.1:p.Leu487=
XM_017020486.1:c.1770C>G	XP_016875975.1:p.Leu590=
XM_017020487.1:c.1461C>G	XP_016875976.1:p.Leu487=
XM_017020488.1:c.1107C>G	XP_016875977.1:p.Leu369=
XM_017020489.1:c.1089C>G	XP_016875978.1:p.Leu363=
NM_004119.3:c.1986C>G MANE Select	NP_004110.2:p.Leu662=
NR_130706.2:n.2052C>G