Canonical Allele Identifier: CA1239264985

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240182_25240183delinsGC , CM000664.2:g.25240182_25240183delinsGC	GRCh38
NC_000002.11:g.25463051_25463052delinsGC , CM000664.1:g.25463051_25463052delinsGC	GRCh37
NC_000002.10:g.25316555_25316556delinsGC	NCBI36
NG_029465.2:g.107408_107409delinsGC , LRG_459:g.107408_107409delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.641+119_641+120delinsGC
ENST00000683393.1:c.1468+119_1468+120delinsGC	ENSP00000508654.1:n.1468+119_1468+120delinsGC
ENST00000683760.1:c.1653+119_1653+120delinsGC	ENSP00000507765.1:n.1653+119_1653+120delinsGC
ENST00000321117.10:c.2322+119_2322+120delinsGC MANE Select	ENSP00000324375.5:n.2322+119_2322+120delinsGC
ENST00000264709.7:c.2322+119_2322+120delinsGC	ENSP00000264709.3:n.2322+119_2322+120delinsGC
ENST00000321117.9:c.2322+119_2322+120delinsGC	ENSP00000324375.5:n.2322+119_2322+120delinsGC
ENST00000380746.8:c.1755+119_1755+120delinsGC	ENSP00000370122.4:n.1755+119_1755+120delinsGC
ENST00000380756.7:c.2322+119_2322+120delinsGC	ENSP00000370132.3:n.2322+119_2322+120delinsGC
ENST00000402667.1:c.1653+119_1653+120delinsGC	ENSP00000384237.1:n.1653+119_1653+120delinsGC
ENST00000461228.1:n.541+119_541+120delinsGC
ENST00000466601.5:n.694+119_694+120delinsGC
ENST00000474887.5:n.641+119_641+120delinsGC
ENST00000482935.5:n.322+119_322+120delinsGC
ENST00000491288.5:n.310+457_310+458delinsGC
NM_022552.4:c.2322+119_2322+120delinsGC , LRG_459t1:c.2322+119_2322+120delinsGC	NP_072046.2:n.2322+119_2322+120delinsGC
NM_153759.3:c.1755+119_1755+120delinsGC , LRG_459t2:c.1755+119_1755+120delinsGC	NP_715640.2:n.1755+119_1755+120delinsGC
NM_175629.2:c.2322+119_2322+120delinsGC , LRG_459t4:c.2322+119_2322+120delinsGC	NP_783328.1:n.2322+119_2322+120delinsGC
XM_005264175.3:c.2322+119_2322+120delinsGC	XP_005264232.1:n.2322+119_2322+120delinsGC
XM_005264177.3:c.1653+119_1653+120delinsGC	XP_005264234.1:n.1653+119_1653+120delinsGC
XM_006711957.2:c.2322+119_2322+120delinsGC	XP_006712020.1:n.2322+119_2322+120delinsGC
XM_006711958.2:c.1878+119_1878+120delinsGC	XP_006712021.1:n.1878+119_1878+120delinsGC
XM_011532662.1:c.2175+119_2175+120delinsGC	XP_011530964.1:n.2175+119_2175+120delinsGC
XM_011532663.1:c.2157+119_2157+120delinsGC	XP_011530965.1:n.2157+119_2157+120delinsGC
XM_011532664.1:c.2322+119_2322+120delinsGC	XP_011530966.1:n.2322+119_2322+120delinsGC
XM_011532665.1:c.1866+119_1866+120delinsGC	XP_011530967.1:n.1866+119_1866+120delinsGC
XM_011532666.1:c.1794+119_1794+120delinsGC	XP_011530968.1:n.1794+119_1794+120delinsGC
XM_011532667.1:c.1653+119_1653+120delinsGC	XP_011530969.1:n.1653+119_1653+120delinsGC
XM_011532668.1:c.2322+119_2322+120delinsGC	XP_011530970.1:n.2322+119_2322+120delinsGC
NM_001320893.1:c.1866+119_1866+120delinsGC	NP_001307822.1:n.1866+119_1866+120delinsGC
NR_135490.1:n.2660+119_2660+120delinsGC
XM_005264175.5:c.2322+119_2322+120delinsGC	XP_005264232.1:n.2322+119_2322+120delinsGC
XM_005264177.4:c.1653+119_1653+120delinsGC	XP_005264234.1:n.1653+119_1653+120delinsGC
XM_011532662.2:c.2175+119_2175+120delinsGC	XP_011530964.1:n.2175+119_2175+120delinsGC
XM_011532663.2:c.2157+119_2157+120delinsGC	XP_011530965.1:n.2157+119_2157+120delinsGC
XM_011532664.2:c.2322+119_2322+120delinsGC	XP_011530966.1:n.2322+119_2322+120delinsGC
XM_011532666.2:c.1794+119_1794+120delinsGC	XP_011530968.1:n.1794+119_1794+120delinsGC
XM_011532667.3:c.1653+119_1653+120delinsGC	XP_011530969.1:n.1653+119_1653+120delinsGC
XM_017003526.1:c.2322+119_2322+120delinsGC	XP_016859015.1:n.2322+119_2322+120delinsGC
XM_017003527.1:c.1653+119_1653+120delinsGC	XP_016859016.1:n.1653+119_1653+120delinsGC
XR_001738657.1:n.2599+119_2599+120delinsGC
NM_001375819.1:c.1653+119_1653+120delinsGC	NP_001362748.1:n.1653+119_1653+120delinsGC
NR_135490.2:n.2553+119_2553+120delinsGC
NM_022552.5:c.2322+119_2322+120delinsGC MANE Select	NP_072046.2:n.2322+119_2322+120delinsGC