Canonical Allele Identifier: CA2658171557

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25240253-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240253A>G , CM000664.2:g.25240253A>G	GRCh38
NC_000002.11:g.25463122A>G , CM000664.1:g.25463122A>G	GRCh37
NC_000002.10:g.25316626A>G	NCBI36
NG_029465.2:g.107338T>C , LRG_459:g.107338T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000474887.6:c.641+49T>C
ENST00000683393.1:c.1468+49T>C	ENSP00000508654.1:n.1468+49T>C
ENST00000683760.1:c.1653+49T>C	ENSP00000507765.1:n.1653+49T>C
ENST00000321117.10:c.2322+49T>C MANE Select	ENSP00000324375.5:n.2322+49T>C
ENST00000264709.7:c.2322+49T>C	ENSP00000264709.3:n.2322+49T>C
ENST00000321117.9:c.2322+49T>C	ENSP00000324375.5:n.2322+49T>C
ENST00000380746.8:c.1755+49T>C	ENSP00000370122.4:n.1755+49T>C
ENST00000380756.7:c.2322+49T>C	ENSP00000370132.3:n.2322+49T>C
ENST00000402667.1:c.1653+49T>C	ENSP00000384237.1:n.1653+49T>C
ENST00000461228.1:n.541+49T>C
ENST00000466601.5:n.694+49T>C
ENST00000474887.5:n.641+49T>C
ENST00000482935.5:n.322+49T>C
ENST00000491288.5:n.310+387T>C
NM_022552.4:c.2322+49T>C , LRG_459t1:c.2322+49T>C	NP_072046.2:n.2322+49T>C
NM_153759.3:c.1755+49T>C , LRG_459t2:c.1755+49T>C	NP_715640.2:n.1755+49T>C
NM_175629.2:c.2322+49T>C , LRG_459t4:c.2322+49T>C	NP_783328.1:n.2322+49T>C
XM_005264175.3:c.2322+49T>C	XP_005264232.1:n.2322+49T>C
XM_005264177.3:c.1653+49T>C	XP_005264234.1:n.1653+49T>C
XM_006711957.2:c.2322+49T>C	XP_006712020.1:n.2322+49T>C
XM_006711958.2:c.1878+49T>C	XP_006712021.1:n.1878+49T>C
XM_011532662.1:c.2175+49T>C	XP_011530964.1:n.2175+49T>C
XM_011532663.1:c.2157+49T>C	XP_011530965.1:n.2157+49T>C
XM_011532664.1:c.2322+49T>C	XP_011530966.1:n.2322+49T>C
XM_011532665.1:c.1866+49T>C	XP_011530967.1:n.1866+49T>C
XM_011532666.1:c.1794+49T>C	XP_011530968.1:n.1794+49T>C
XM_011532667.1:c.1653+49T>C	XP_011530969.1:n.1653+49T>C
XM_011532668.1:c.2322+49T>C	XP_011530970.1:n.2322+49T>C
NM_001320893.1:c.1866+49T>C	NP_001307822.1:n.1866+49T>C
NR_135490.1:n.2660+49T>C
XM_005264175.5:c.2322+49T>C	XP_005264232.1:n.2322+49T>C
XM_005264177.4:c.1653+49T>C	XP_005264234.1:n.1653+49T>C
XM_011532662.2:c.2175+49T>C	XP_011530964.1:n.2175+49T>C
XM_011532663.2:c.2157+49T>C	XP_011530965.1:n.2157+49T>C
XM_011532664.2:c.2322+49T>C	XP_011530966.1:n.2322+49T>C
XM_011532666.2:c.1794+49T>C	XP_011530968.1:n.1794+49T>C
XM_011532667.3:c.1653+49T>C	XP_011530969.1:n.1653+49T>C
XM_017003526.1:c.2322+49T>C	XP_016859015.1:n.2322+49T>C
XM_017003527.1:c.1653+49T>C	XP_016859016.1:n.1653+49T>C
XR_001738657.1:n.2599+49T>C
NM_001375819.1:c.1653+49T>C	NP_001362748.1:n.1653+49T>C
NR_135490.2:n.2553+49T>C
NM_022552.5:c.2322+49T>C MANE Select	NP_072046.2:n.2322+49T>C