Canonical Allele Identifier: CA1555916

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244539C>T , CM000664.2:g.25244539C>T	GRCh38
NC_000002.11:g.25467408C>T , CM000664.1:g.25467408C>T	GRCh37
NC_000002.10:g.25320912C>T	NCBI36
NG_029465.2:g.103052G>A , LRG_459:g.103052G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022552.5:c.1667+1G>A MANE Select	NP_072046.2:n.1667+1G>A
ENST00000321117.10:c.1667+1G>A MANE Select	ENSP00000324375.5:n.1667+1G>A
NM_001320893.1:c.1211+1G>A	NP_001307822.1:n.1211+1G>A
NM_001375819.1:c.998+1G>A	NP_001362748.1:n.998+1G>A
NM_022552.4:c.1667+1G>A , LRG_459t1:c.1667+1G>A	NP_072046.2:n.1667+1G>A
NM_153759.3:c.1100+1G>A , LRG_459t2:c.1100+1G>A	NP_715640.2:n.1100+1G>A
NM_175629.2:c.1667+1G>A , LRG_459t4:c.1667+1G>A	NP_783328.1:n.1667+1G>A
NR_135490.1:n.2005+1G>A
NR_135490.2:n.1898+1G>A
ENST00000264709.7:c.1667+1G>A	ENSP00000264709.3:n.1667+1G>A
ENST00000321117.9:c.1667+1G>A	ENSP00000324375.5:n.1667+1G>A
ENST00000380746.8:c.1100+1G>A	ENSP00000370122.4:n.1100+1G>A
ENST00000380756.7:c.1667+1G>A	ENSP00000370132.3:n.1667+1G>A
ENST00000402667.1:c.998+1G>A	ENSP00000384237.1:n.998+1G>A
ENST00000683393.1:c.813+1G>A	ENSP00000508654.1:n.813+1G>A
ENST00000683760.1:c.998+1G>A	ENSP00000507765.1:n.998+1G>A
XM_005264175.3:c.1667+1G>A	XP_005264232.1:n.1667+1G>A
XM_005264175.5:c.1667+1G>A	XP_005264232.1:n.1667+1G>A
XM_005264177.3:c.998+1G>A	XP_005264234.1:n.998+1G>A
XM_005264177.4:c.998+1G>A	XP_005264234.1:n.998+1G>A
XM_006711957.2:c.1667+1G>A	XP_006712020.1:n.1667+1G>A
XM_006711958.2:c.1223+1G>A	XP_006712021.1:n.1223+1G>A
XM_011532662.1:c.1520+1G>A	XP_011530964.1:n.1520+1G>A
XM_011532662.2:c.1520+1G>A	XP_011530964.1:n.1520+1G>A
XM_011532663.1:c.1502+1G>A	XP_011530965.1:n.1502+1G>A
XM_011532663.2:c.1502+1G>A	XP_011530965.1:n.1502+1G>A
XM_011532664.1:c.1667+1G>A	XP_011530966.1:n.1667+1G>A
XM_011532664.2:c.1667+1G>A	XP_011530966.1:n.1667+1G>A
XM_011532665.1:c.1211+1G>A	XP_011530967.1:n.1211+1G>A
XM_011532666.1:c.1139+1G>A	XP_011530968.1:n.1139+1G>A
XM_011532666.2:c.1139+1G>A	XP_011530968.1:n.1139+1G>A
XM_011532667.1:c.998+1G>A	XP_011530969.1:n.998+1G>A
XM_011532667.3:c.998+1G>A	XP_011530969.1:n.998+1G>A
XM_011532668.1:c.1667+1G>A	XP_011530970.1:n.1667+1G>A
XM_017003526.1:c.1667+1G>A	XP_016859015.1:n.1667+1G>A
XM_017003527.1:c.998+1G>A	XP_016859016.1:n.998+1G>A
XR_001738657.1:n.1944+1G>A