Canonical Allele Identifier: CA2622472648

Gene: FLT3

Linked Data

• gnomAD v4: 13-28028061-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028061T>C , CM000675.2:g.28028061T>C	GRCh38
NC_000013.10:g.28602198T>C , CM000675.1:g.28602198T>C	GRCh37
NC_000013.9:g.27500198T>C	NCBI36
NG_007066.1:g.77508A>G , LRG_457:g.77508A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2053+117A>G MANE Select	ENSP00000241453.7:n.2053+117A>G
ENST00000241453.11:c.2053+117A>G	ENSP00000241453.7:n.2053+117A>G
ENST00000380987.2:c.2053+117A>G	ENSP00000370374.2:n.2053+117A>G
NM_004119.2:c.2053+117A>G , LRG_457t1:c.2053+117A>G	NP_004110.2:n.2053+117A>G
NR_130706.1:n.2135+117A>G
XM_011535015.1:c.1996+117A>G	XP_011533317.1:n.1996+117A>G
XM_011535016.1:c.1528+117A>G	XP_011533318.1:n.1528+117A>G
XM_011535017.1:c.1528+117A>G	XP_011533319.1:n.1528+117A>G
XM_011535018.1:c.1528+117A>G	XP_011533320.1:n.1528+117A>G
XM_011535015.2:c.1996+117A>G	XP_011533317.1:n.1996+117A>G
XM_011535017.2:c.1528+117A>G	XP_011533319.1:n.1528+117A>G
XM_011535018.2:c.1528+117A>G	XP_011533320.1:n.1528+117A>G
XM_017020486.1:c.1837+117A>G	XP_016875975.1:n.1837+117A>G
XM_017020487.1:c.1528+117A>G	XP_016875976.1:n.1528+117A>G
XM_017020488.1:c.1174+117A>G	XP_016875977.1:n.1174+117A>G
XM_017020489.1:c.1156+117A>G	XP_016875978.1:n.1156+117A>G
NM_004119.3:c.2053+117A>G MANE Select	NP_004110.2:n.2053+117A>G
NR_130706.2:n.2119+117A>G