Canonical Allele Identifier: CA387641068

Gene: FLT3

Linked Data

• dbSNP Id: rs2137676037
• MyVariant Identifiers: chr13:g.28608333G>A (hg19) ; chr13:g.28034196G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034196G>A , CM000675.2:g.28034196G>A	GRCh38
NC_000013.10:g.28608333G>A , CM000675.1:g.28608333G>A	GRCh37
NC_000013.9:g.27506333G>A	NCBI36
NG_007066.1:g.71373C>T , LRG_457:g.71373C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1723C>T MANE Select	ENSP00000241453.7:p.Gln575Ter
ENST00000241453.11:c.1723C>T	ENSP00000241453.7:p.Gln575Ter
ENST00000380987.2:c.1723C>T	ENSP00000370374.2:p.Gln575Ter
NM_004119.2:c.1723C>T , LRG_457t1:c.1723C>T	NP_004110.2:p.Gln575Ter
NR_130706.1:n.1805C>T
XM_011535015.1:c.1666C>T	XP_011533317.1:p.Gln556Ter
XM_011535016.1:c.1198C>T	XP_011533318.1:p.Gln400Ter
XM_011535017.1:c.1198C>T	XP_011533319.1:p.Gln400Ter
XM_011535018.1:c.1198C>T	XP_011533320.1:p.Gln400Ter
XM_011535015.2:c.1666C>T	XP_011533317.1:p.Gln556Ter
XM_011535017.2:c.1198C>T	XP_011533319.1:p.Gln400Ter
XM_011535018.2:c.1198C>T	XP_011533320.1:p.Gln400Ter
XM_017020486.1:c.1507C>T	XP_016875975.1:p.Gln503Ter
XM_017020487.1:c.1198C>T	XP_016875976.1:p.Gln400Ter
XM_017020488.1:c.844C>T	XP_016875977.1:p.Gln282Ter
XM_017020489.1:c.826C>T	XP_016875978.1:p.Gln276Ter
NM_004119.3:c.1723C>T MANE Select	NP_004110.2:p.Gln575Ter
NR_130706.2:n.1789C>T