Canonical Allele Identifier: CA2080790601

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028203G= , CM000675.2:g.28028203G=	GRCh38
NC_000013.10:g.28602340G= , CM000675.1:g.28602340G=	GRCh37
NC_000013.9:g.27500340G=	NCBI36
NG_007066.1:g.77366C= , LRG_457:g.77366C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2028C= MANE Select	ENSP00000241453.7:p.Asn676=
ENST00000241453.11:c.2028C=	ENSP00000241453.7:p.Asn676=
ENST00000380987.2:c.2028C=	ENSP00000370374.2:p.Asn676=
NM_004119.2:c.2028C= , LRG_457t1:c.2028C=	NP_004110.2:p.Asn676=
NR_130706.1:n.2110C=
XM_011535015.1:c.1971C=	XP_011533317.1:p.Asn657=
XM_011535016.1:c.1503C=	XP_011533318.1:p.Asn501=
XM_011535017.1:c.1503C=	XP_011533319.1:p.Asn501=
XM_011535018.1:c.1503C=	XP_011533320.1:p.Asn501=
XM_011535015.2:c.1971C=	XP_011533317.1:p.Asn657=
XM_011535017.2:c.1503C=	XP_011533319.1:p.Asn501=
XM_011535018.2:c.1503C=	XP_011533320.1:p.Asn501=
XM_017020486.1:c.1812C=	XP_016875975.1:p.Asn604=
XM_017020487.1:c.1503C=	XP_016875976.1:p.Asn501=
XM_017020488.1:c.1149C=	XP_016875977.1:p.Asn383=
XM_017020489.1:c.1131C=	XP_016875978.1:p.Asn377=
NM_004119.3:c.2028C= MANE Select	NP_004110.2:p.Asn676=
NR_130706.2:n.2094C=