Canonical Allele Identifier: CA387640902

Gene: FLT3

Linked Data

• dbSNP Id: rs2137675507
• gnomAD v4: 13-28034162-T-C
• MyVariant Identifiers: chr13:g.28608299T>C (hg19) ; chr13:g.28034162T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034162T>C , CM000675.2:g.28034162T>C	GRCh38
NC_000013.10:g.28608299T>C , CM000675.1:g.28608299T>C	GRCh37
NC_000013.9:g.27506299T>C	NCBI36
NG_007066.1:g.71407A>G , LRG_457:g.71407A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1757A>G MANE Select	ENSP00000241453.7:p.Asp586Gly
ENST00000241453.11:c.1757A>G	ENSP00000241453.7:p.Asp586Gly
ENST00000380987.2:c.1757A>G	ENSP00000370374.2:p.Asp586Gly
NM_004119.2:c.1757A>G , LRG_457t1:c.1757A>G	NP_004110.2:p.Asp586Gly
NR_130706.1:n.1839A>G
XM_011535015.1:c.1700A>G	XP_011533317.1:p.Asp567Gly
XM_011535016.1:c.1232A>G	XP_011533318.1:p.Asp411Gly
XM_011535017.1:c.1232A>G	XP_011533319.1:p.Asp411Gly
XM_011535018.1:c.1232A>G	XP_011533320.1:p.Asp411Gly
XM_011535015.2:c.1700A>G	XP_011533317.1:p.Asp567Gly
XM_011535017.2:c.1232A>G	XP_011533319.1:p.Asp411Gly
XM_011535018.2:c.1232A>G	XP_011533320.1:p.Asp411Gly
XM_017020486.1:c.1541A>G	XP_016875975.1:p.Asp514Gly
XM_017020487.1:c.1232A>G	XP_016875976.1:p.Asp411Gly
XM_017020488.1:c.878A>G	XP_016875977.1:p.Asp293Gly
XM_017020489.1:c.860A>G	XP_016875978.1:p.Asp287Gly
NM_004119.3:c.1757A>G MANE Select	NP_004110.2:p.Asp586Gly
NR_130706.2:n.1823A>G