Canonical Allele Identifier: CA387652130

Gene: FLT3

Linked Data

• COSMIC: COSM5879388
• MyVariant Identifiers: chr13:g.28602341T>G (hg19) ; chr13:g.28028204T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028204T>G , CM000675.2:g.28028204T>G	GRCh38
NC_000013.10:g.28602341T>G , CM000675.1:g.28602341T>G	GRCh37
NC_000013.9:g.27500341T>G	NCBI36
NG_007066.1:g.77365A>C , LRG_457:g.77365A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2027A>C MANE Select	ENSP00000241453.7:p.Asn676Thr
ENST00000241453.11:c.2027A>C	ENSP00000241453.7:p.Asn676Thr
ENST00000380987.2:c.2027A>C	ENSP00000370374.2:p.Asn676Thr
NM_004119.2:c.2027A>C , LRG_457t1:c.2027A>C	NP_004110.2:p.Asn676Thr
NR_130706.1:n.2109A>C
XM_011535015.1:c.1970A>C	XP_011533317.1:p.Asn657Thr
XM_011535016.1:c.1502A>C	XP_011533318.1:p.Asn501Thr
XM_011535017.1:c.1502A>C	XP_011533319.1:p.Asn501Thr
XM_011535018.1:c.1502A>C	XP_011533320.1:p.Asn501Thr
XM_011535015.2:c.1970A>C	XP_011533317.1:p.Asn657Thr
XM_011535017.2:c.1502A>C	XP_011533319.1:p.Asn501Thr
XM_011535018.2:c.1502A>C	XP_011533320.1:p.Asn501Thr
XM_017020486.1:c.1811A>C	XP_016875975.1:p.Asn604Thr
XM_017020487.1:c.1502A>C	XP_016875976.1:p.Asn501Thr
XM_017020488.1:c.1148A>C	XP_016875977.1:p.Asn383Thr
XM_017020489.1:c.1130A>C	XP_016875978.1:p.Asn377Thr
NM_004119.3:c.2027A>C MANE Select	NP_004110.2:p.Asn676Thr
NR_130706.2:n.2093A>C