Canonical Allele Identifier: CA387652162

Gene: FLT3

Linked Data

• dbSNP Id: rs149216274
• gnomAD v2: 13-28602355-G-C
• MyVariant Identifiers: chr13:g.28602355G>C (hg19) ; chr13:g.28028218G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028218G>C , CM000675.2:g.28028218G>C	GRCh38
NC_000013.10:g.28602355G>C , CM000675.1:g.28602355G>C	GRCh37
NC_000013.9:g.27500355G>C	NCBI36
NG_007066.1:g.77351C>G , LRG_457:g.77351C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2013C>G MANE Select	ENSP00000241453.7:p.His671Gln
ENST00000241453.11:c.2013C>G	ENSP00000241453.7:p.His671Gln
ENST00000380987.2:c.2013C>G	ENSP00000370374.2:p.His671Gln
NM_004119.2:c.2013C>G , LRG_457t1:c.2013C>G	NP_004110.2:p.His671Gln
NR_130706.1:n.2095C>G
XM_011535015.1:c.1956C>G	XP_011533317.1:p.His652Gln
XM_011535016.1:c.1488C>G	XP_011533318.1:p.His496Gln
XM_011535017.1:c.1488C>G	XP_011533319.1:p.His496Gln
XM_011535018.1:c.1488C>G	XP_011533320.1:p.His496Gln
XM_011535015.2:c.1956C>G	XP_011533317.1:p.His652Gln
XM_011535017.2:c.1488C>G	XP_011533319.1:p.His496Gln
XM_011535018.2:c.1488C>G	XP_011533320.1:p.His496Gln
XM_017020486.1:c.1797C>G	XP_016875975.1:p.His599Gln
XM_017020487.1:c.1488C>G	XP_016875976.1:p.His496Gln
XM_017020488.1:c.1134C>G	XP_016875977.1:p.His378Gln
XM_017020489.1:c.1116C>G	XP_016875978.1:p.His372Gln
NM_004119.3:c.2013C>G MANE Select	NP_004110.2:p.His671Gln
NR_130706.2:n.2079C>G