Canonical Allele Identifier: CA387652150

Gene: FLT3

Linked Data

• MyVariant Identifiers: chr13:g.28602350T>G (hg19) ; chr13:g.28028213T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028213T>G , CM000675.2:g.28028213T>G	GRCh38
NC_000013.10:g.28602350T>G , CM000675.1:g.28602350T>G	GRCh37
NC_000013.9:g.27500350T>G	NCBI36
NG_007066.1:g.77356A>C , LRG_457:g.77356A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2018A>C MANE Select	ENSP00000241453.7:p.Asn673Thr
ENST00000241453.11:c.2018A>C	ENSP00000241453.7:p.Asn673Thr
ENST00000380987.2:c.2018A>C	ENSP00000370374.2:p.Asn673Thr
NM_004119.2:c.2018A>C , LRG_457t1:c.2018A>C	NP_004110.2:p.Asn673Thr
NR_130706.1:n.2100A>C
XM_011535015.1:c.1961A>C	XP_011533317.1:p.Asn654Thr
XM_011535016.1:c.1493A>C	XP_011533318.1:p.Asn498Thr
XM_011535017.1:c.1493A>C	XP_011533319.1:p.Asn498Thr
XM_011535018.1:c.1493A>C	XP_011533320.1:p.Asn498Thr
XM_011535015.2:c.1961A>C	XP_011533317.1:p.Asn654Thr
XM_011535017.2:c.1493A>C	XP_011533319.1:p.Asn498Thr
XM_011535018.2:c.1493A>C	XP_011533320.1:p.Asn498Thr
XM_017020486.1:c.1802A>C	XP_016875975.1:p.Asn601Thr
XM_017020487.1:c.1493A>C	XP_016875976.1:p.Asn498Thr
XM_017020488.1:c.1139A>C	XP_016875977.1:p.Asn380Thr
XM_017020489.1:c.1121A>C	XP_016875978.1:p.Asn374Thr
NM_004119.3:c.2018A>C MANE Select	NP_004110.2:p.Asn673Thr
NR_130706.2:n.2084A>C