Canonical Allele Identifier: CA6928484

Gene: FLT3

Linked Data

• dbSNP Id: rs375553856
• ExAC: 13:28602343 C / G
• gnomAD v2: 13-28602343-C-G
• MyVariant Identifiers: chr13:g.28602343C>G (hg19) ; chr13:g.28028206C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028206C>G , CM000675.2:g.28028206C>G	GRCh38
NC_000013.10:g.28602343C>G , CM000675.1:g.28602343C>G	GRCh37
NC_000013.9:g.27500343C>G	NCBI36
NG_007066.1:g.77363G>C , LRG_457:g.77363G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2025G>C MANE Select	ENSP00000241453.7:p.Val675=
ENST00000241453.11:c.2025G>C	ENSP00000241453.7:p.Val675=
ENST00000380987.2:c.2025G>C	ENSP00000370374.2:p.Val675=
NM_004119.2:c.2025G>C , LRG_457t1:c.2025G>C	NP_004110.2:p.Val675=
NR_130706.1:n.2107G>C
XM_011535015.1:c.1968G>C	XP_011533317.1:p.Val656=
XM_011535016.1:c.1500G>C	XP_011533318.1:p.Val500=
XM_011535017.1:c.1500G>C	XP_011533319.1:p.Val500=
XM_011535018.1:c.1500G>C	XP_011533320.1:p.Val500=
XM_011535015.2:c.1968G>C	XP_011533317.1:p.Val656=
XM_011535017.2:c.1500G>C	XP_011533319.1:p.Val500=
XM_011535018.2:c.1500G>C	XP_011533320.1:p.Val500=
XM_017020486.1:c.1809G>C	XP_016875975.1:p.Val603=
XM_017020487.1:c.1500G>C	XP_016875976.1:p.Val500=
XM_017020488.1:c.1146G>C	XP_016875977.1:p.Val382=
XM_017020489.1:c.1128G>C	XP_016875978.1:p.Val376=
NM_004119.3:c.2025G>C MANE Select	NP_004110.2:p.Val675=
NR_130706.2:n.2091G>C