Canonical Allele Identifier: CA6928474

Gene: FLT3

Linked Data

• ClinVar Variation Id: 1291612
• ClinVar RCV Id: RCV001713507
• dbSNP Id: rs75580865
• ExAC: 13:28602292 T / C
• gnomAD v2: 13-28602292-T-C
• gnomAD v3: 13-28028155-T-C
• gnomAD v4: 13-28028155-T-C
• MyVariant Identifiers: chr13:g.28602292T>C (hg19) ; chr13:g.28028155T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028155T>C , CM000675.2:g.28028155T>C	GRCh38
NC_000013.10:g.28602292T>C , CM000675.1:g.28602292T>C	GRCh37
NC_000013.9:g.27500292T>C	NCBI36
NG_007066.1:g.77414A>G , LRG_457:g.77414A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2053+23A>G MANE Select	ENSP00000241453.7:n.2053+23A>G
ENST00000241453.11:c.2053+23A>G	ENSP00000241453.7:n.2053+23A>G
ENST00000380987.2:c.2053+23A>G	ENSP00000370374.2:n.2053+23A>G
NM_004119.2:c.2053+23A>G , LRG_457t1:c.2053+23A>G	NP_004110.2:n.2053+23A>G
NR_130706.1:n.2135+23A>G
XM_011535015.1:c.1996+23A>G	XP_011533317.1:n.1996+23A>G
XM_011535016.1:c.1528+23A>G	XP_011533318.1:n.1528+23A>G
XM_011535017.1:c.1528+23A>G	XP_011533319.1:n.1528+23A>G
XM_011535018.1:c.1528+23A>G	XP_011533320.1:n.1528+23A>G
XM_011535015.2:c.1996+23A>G	XP_011533317.1:n.1996+23A>G
XM_011535017.2:c.1528+23A>G	XP_011533319.1:n.1528+23A>G
XM_011535018.2:c.1528+23A>G	XP_011533320.1:n.1528+23A>G
XM_017020486.1:c.1837+23A>G	XP_016875975.1:n.1837+23A>G
XM_017020487.1:c.1528+23A>G	XP_016875976.1:n.1528+23A>G
XM_017020488.1:c.1174+23A>G	XP_016875977.1:n.1174+23A>G
XM_017020489.1:c.1156+23A>G	XP_016875978.1:n.1156+23A>G
NM_004119.3:c.2053+23A>G MANE Select	NP_004110.2:n.2053+23A>G
NR_130706.2:n.2119+23A>G