Canonical Allele Identifier: CA2080790617

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028251T= , CM000675.2:g.28028251T=	GRCh38
NC_000013.10:g.28602388T= , CM000675.1:g.28602388T=	GRCh37
NC_000013.9:g.27500388T=	NCBI36
NG_007066.1:g.77318A= , LRG_457:g.77318A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1980A= MANE Select	ENSP00000241453.7:p.Ser660=
ENST00000241453.11:c.1980A=	ENSP00000241453.7:p.Ser660=
ENST00000380987.2:c.1980A=	ENSP00000370374.2:p.Ser660=
NM_004119.2:c.1980A= , LRG_457t1:c.1980A=	NP_004110.2:p.Ser660=
NR_130706.1:n.2062A=
XM_011535015.1:c.1923A=	XP_011533317.1:p.Ser641=
XM_011535016.1:c.1455A=	XP_011533318.1:p.Ser485=
XM_011535017.1:c.1455A=	XP_011533319.1:p.Ser485=
XM_011535018.1:c.1455A=	XP_011533320.1:p.Ser485=
XM_011535015.2:c.1923A=	XP_011533317.1:p.Ser641=
XM_011535017.2:c.1455A=	XP_011533319.1:p.Ser485=
XM_011535018.2:c.1455A=	XP_011533320.1:p.Ser485=
XM_017020486.1:c.1764A=	XP_016875975.1:p.Ser588=
XM_017020487.1:c.1455A=	XP_016875976.1:p.Ser485=
XM_017020488.1:c.1101A=	XP_016875977.1:p.Ser367=
XM_017020489.1:c.1083A=	XP_016875978.1:p.Ser361=
NM_004119.3:c.1980A= MANE Select	NP_004110.2:p.Ser660=
NR_130706.2:n.2046A=