Canonical Allele Identifier: CA387652135

Gene: FLT3

Linked Data

• gnomAD v4: 13-28028207-A-G
• COSMIC: COSM6342215
• MyVariant Identifiers: chr13:g.28602344A>G (hg19) ; chr13:g.28028207A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028207A>G , CM000675.2:g.28028207A>G	GRCh38
NC_000013.10:g.28602344A>G , CM000675.1:g.28602344A>G	GRCh37
NC_000013.9:g.27500344A>G	NCBI36
NG_007066.1:g.77362T>C , LRG_457:g.77362T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2024T>C MANE Select	ENSP00000241453.7:p.Val675Ala
ENST00000241453.11:c.2024T>C	ENSP00000241453.7:p.Val675Ala
ENST00000380987.2:c.2024T>C	ENSP00000370374.2:p.Val675Ala
NM_004119.2:c.2024T>C , LRG_457t1:c.2024T>C	NP_004110.2:p.Val675Ala
NR_130706.1:n.2106T>C
XM_011535015.1:c.1967T>C	XP_011533317.1:p.Val656Ala
XM_011535016.1:c.1499T>C	XP_011533318.1:p.Val500Ala
XM_011535017.1:c.1499T>C	XP_011533319.1:p.Val500Ala
XM_011535018.1:c.1499T>C	XP_011533320.1:p.Val500Ala
XM_011535015.2:c.1967T>C	XP_011533317.1:p.Val656Ala
XM_011535017.2:c.1499T>C	XP_011533319.1:p.Val500Ala
XM_011535018.2:c.1499T>C	XP_011533320.1:p.Val500Ala
XM_017020486.1:c.1808T>C	XP_016875975.1:p.Val603Ala
XM_017020487.1:c.1499T>C	XP_016875976.1:p.Val500Ala
XM_017020488.1:c.1145T>C	XP_016875977.1:p.Val382Ala
XM_017020489.1:c.1127T>C	XP_016875978.1:p.Val376Ala
NM_004119.3:c.2024T>C MANE Select	NP_004110.2:p.Val675Ala
NR_130706.2:n.2090T>C