Canonical Allele Identifier: CA16602569
Gene: FLT3 HGNC NCBI

Linked Data

ClinVar Variation Id: 376110
ClinVar RCV Id: RCV000443164
dbSNP Id: rs1057519767
MyVariant Identifiers: chr13:g.28602342T>C (hg19) chr13:g.28028205T>C (hg38)
PubMed: PMID:22504184 PMID:23430109 PMID:24619500
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28028205T>C , CM000675.2:g.28028205T>C GRCh38
NC_000013.10:g.28602342T>C , CM000675.1:g.28602342T>C GRCh37
NC_000013.9:g.27500342T>C NCBI36
NG_007066.1:g.77364A>G , LRG_457:g.77364A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000241453.12:c.2026A>G MANE Select ENSP00000241453.7:p.Asn676Asp
ENST00000241453.11:c.2026A>G ENSP00000241453.7:p.Asn676Asp
ENST00000380987.2:c.2026A>G ENSP00000370374.2:p.Asn676Asp
NM_004119.2:c.2026A>G , LRG_457t1:c.2026A>G NP_004110.2:p.Asn676Asp
NR_130706.1:n.2108A>G
XM_011535015.1:c.1969A>G XP_011533317.1:p.Asn657Asp
XM_011535016.1:c.1501A>G XP_011533318.1:p.Asn501Asp
XM_011535017.1:c.1501A>G XP_011533319.1:p.Asn501Asp
XM_011535018.1:c.1501A>G XP_011533320.1:p.Asn501Asp
XM_011535015.2:c.1969A>G XP_011533317.1:p.Asn657Asp
XM_011535017.2:c.1501A>G XP_011533319.1:p.Asn501Asp
XM_011535018.2:c.1501A>G XP_011533320.1:p.Asn501Asp
XM_017020486.1:c.1810A>G XP_016875975.1:p.Asn604Asp
XM_017020487.1:c.1501A>G XP_016875976.1:p.Asn501Asp
XM_017020488.1:c.1147A>G XP_016875977.1:p.Asn383Asp
XM_017020489.1:c.1129A>G XP_016875978.1:p.Asn377Asp
NM_004119.3:c.2026A>G MANE Select NP_004110.2:p.Asn676Asp
NR_130706.2:n.2092A>G
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