Canonical Allele Identifier: CA425181393

Gene: DNMT3A

Linked Data

• dbSNP Id: rs1553410528
• gnomAD v2: 2-25463174-G-C
• gnomAD v4: 2-25240305-G-C
• MyVariant Identifiers: chr2:g.25463174G>C (hg19) ; chr2:g.25463174_25463188delinsCAGAAATCGCGAGAT (hg19) ; chr2:g.25240305_25240319delinsCAGAAATCGCGAGAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240305G>C , CM000664.2:g.25240305G>C	GRCh38
NC_000002.11:g.25463174G>C , CM000664.1:g.25463174G>C	GRCh37
NC_000002.10:g.25316678G>C	NCBI36
NG_029465.2:g.107286C>G , LRG_459:g.107286C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.638C>G
ENST00000683393.1:c.1465C>G	ENSP00000508654.1:n.1465C>G
ENST00000683760.1:c.1650C>G	ENSP00000507765.1:p.Leu550=
ENST00000321117.10:c.2319C>G MANE Select	ENSP00000324375.5:p.Leu773=
ENST00000264709.7:c.2319C>G	ENSP00000264709.3:p.Leu773=
ENST00000321117.9:c.2319C>G	ENSP00000324375.5:p.Leu773=
ENST00000380746.8:c.1752C>G	ENSP00000370122.4:p.Leu584=
ENST00000380756.7:c.2319C>G	ENSP00000370132.3:p.Leu773=
ENST00000402667.1:c.1650C>G	ENSP00000384237.1:p.Leu550=
ENST00000461228.1:n.538C>G
ENST00000466601.5:n.691C>G
ENST00000474887.5:n.638C>G
ENST00000482935.5:n.319C>G
ENST00000491288.5:n.310+335C>G
NM_022552.4:c.2319C>G , LRG_459t1:c.2319C>G	NP_072046.2:p.Leu773=
NM_153759.3:c.1752C>G , LRG_459t2:c.1752C>G	NP_715640.2:p.Leu584=
NM_175629.2:c.2319C>G , LRG_459t4:c.2319C>G	NP_783328.1:p.Leu773=
XM_005264175.3:c.2319C>G	XP_005264232.1:p.Leu773=
XM_005264177.3:c.1650C>G	XP_005264234.1:p.Leu550=
XM_006711957.2:c.2319C>G	XP_006712020.1:p.Leu773=
XM_006711958.2:c.1875C>G	XP_006712021.1:p.Leu625=
XM_011532662.1:c.2172C>G	XP_011530964.1:p.Leu724=
XM_011532663.1:c.2154C>G	XP_011530965.1:p.Leu718=
XM_011532664.1:c.2319C>G	XP_011530966.1:p.Leu773=
XM_011532665.1:c.1863C>G	XP_011530967.1:p.Leu621=
XM_011532666.1:c.1791C>G	XP_011530968.1:p.Leu597=
XM_011532667.1:c.1650C>G	XP_011530969.1:p.Leu550=
XM_011532668.1:c.2319C>G	XP_011530970.1:p.Leu773=
NM_001320893.1:c.1863C>G	NP_001307822.1:p.Leu621=
NR_135490.1:n.2657C>G
XM_005264175.5:c.2319C>G	XP_005264232.1:p.Leu773=
XM_005264177.4:c.1650C>G	XP_005264234.1:p.Leu550=
XM_011532662.2:c.2172C>G	XP_011530964.1:p.Leu724=
XM_011532663.2:c.2154C>G	XP_011530965.1:p.Leu718=
XM_011532664.2:c.2319C>G	XP_011530966.1:p.Leu773=
XM_011532666.2:c.1791C>G	XP_011530968.1:p.Leu597=
XM_011532667.3:c.1650C>G	XP_011530969.1:p.Leu550=
XM_017003526.1:c.2319C>G	XP_016859015.1:p.Leu773=
XM_017003527.1:c.1650C>G	XP_016859016.1:p.Leu550=
XR_001738657.1:n.2596C>G
NM_001375819.1:c.1650C>G	NP_001362748.1:p.Leu550=
NR_135490.2:n.2550C>G
NM_022552.5:c.2319C>G MANE Select	NP_072046.2:p.Leu773=