Canonical Allele Identifier: CA2576693831

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25246539T>C , CM000664.2:g.25246539T>C	GRCh38
NC_000002.11:g.25469408T>C , CM000664.1:g.25469408T>C	GRCh37
NC_000002.10:g.25322912T>C	NCBI36
NG_029465.2:g.101052A>G , LRG_459:g.101052A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683393.1:c.425+81A>G	ENSP00000508654.1:n.425+81A>G
ENST00000683760.1:c.610+81A>G	ENSP00000507765.1:n.610+81A>G
ENST00000321117.10:c.1279+81A>G MANE Select	ENSP00000324375.5:n.1279+81A>G
ENST00000264709.7:c.1279+81A>G	ENSP00000264709.3:n.1279+81A>G
ENST00000321117.9:c.1279+81A>G	ENSP00000324375.5:n.1279+81A>G
ENST00000380746.8:c.712+81A>G	ENSP00000370122.4:n.712+81A>G
ENST00000380756.7:c.1279+81A>G	ENSP00000370132.3:n.1279+81A>G
ENST00000402667.1:c.610+81A>G	ENSP00000384237.1:n.610+81A>G
ENST00000474807.5:n.574+81A>G
NM_022552.4:c.1279+81A>G , LRG_459t1:c.1279+81A>G	NP_072046.2:n.1279+81A>G
NM_153759.3:c.712+81A>G , LRG_459t2:c.712+81A>G	NP_715640.2:n.712+81A>G
NM_175629.2:c.1279+81A>G , LRG_459t4:c.1279+81A>G	NP_783328.1:n.1279+81A>G
XM_005264175.3:c.1279+81A>G	XP_005264232.1:n.1279+81A>G
XM_005264177.3:c.610+81A>G	XP_005264234.1:n.610+81A>G
XM_006711957.2:c.1279+81A>G	XP_006712020.1:n.1279+81A>G
XM_006711958.2:c.835+81A>G	XP_006712021.1:n.835+81A>G
XM_011532662.1:c.1132+81A>G	XP_011530964.1:n.1132+81A>G
XM_011532663.1:c.1114+81A>G	XP_011530965.1:n.1114+81A>G
XM_011532664.1:c.1279+81A>G	XP_011530966.1:n.1279+81A>G
XM_011532665.1:c.823+81A>G	XP_011530967.1:n.823+81A>G
XM_011532666.1:c.751+81A>G	XP_011530968.1:n.751+81A>G
XM_011532667.1:c.610+81A>G	XP_011530969.1:n.610+81A>G
XM_011532668.1:c.1279+81A>G	XP_011530970.1:n.1279+81A>G
NM_001320893.1:c.823+81A>G	NP_001307822.1:n.823+81A>G
NR_135490.1:n.1617+81A>G
XM_005264175.5:c.1279+81A>G	XP_005264232.1:n.1279+81A>G
XM_005264177.4:c.610+81A>G	XP_005264234.1:n.610+81A>G
XM_011532662.2:c.1132+81A>G	XP_011530964.1:n.1132+81A>G
XM_011532663.2:c.1114+81A>G	XP_011530965.1:n.1114+81A>G
XM_011532664.2:c.1279+81A>G	XP_011530966.1:n.1279+81A>G
XM_011532666.2:c.751+81A>G	XP_011530968.1:n.751+81A>G
XM_011532667.3:c.610+81A>G	XP_011530969.1:n.610+81A>G
XM_017003526.1:c.1279+81A>G	XP_016859015.1:n.1279+81A>G
XM_017003527.1:c.610+81A>G	XP_016859016.1:n.610+81A>G
XR_001738657.1:n.1556+81A>G
NM_001375819.1:c.610+81A>G	NP_001362748.1:n.610+81A>G
NR_135490.2:n.1510+81A>G
NM_022552.5:c.1279+81A>G MANE Select	NP_072046.2:n.1279+81A>G