Canonical Allele Identifier: CA346082861

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25274951C>T , CM000664.2:g.25274951C>T	GRCh38
NC_000002.11:g.25497820C>T , CM000664.1:g.25497820C>T	GRCh37
NC_000002.10:g.25351324C>T	NCBI36
NG_029465.2:g.72640G>A , LRG_459:g.72640G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022552.5:c.629G>A MANE Select	NP_072046.2:p.Trp210Ter
ENST00000321117.10:c.629G>A MANE Select	ENSP00000324375.5:p.Trp210Ter
NM_022552.4:c.629G>A , LRG_459t1:c.629G>A	NP_072046.2:p.Trp210Ter
NM_175629.2:c.629G>A , LRG_459t4:c.629G>A	NP_783328.1:p.Trp210Ter
NR_135490.1:n.967G>A
NR_135490.2:n.860G>A
ENST00000264709.7:c.629G>A	ENSP00000264709.3:p.Trp210Ter
ENST00000321117.9:c.629G>A	ENSP00000324375.5:p.Trp210Ter
ENST00000380756.7:c.629G>A	ENSP00000370132.3:p.Trp210Ter
ENST00000682842.1:n.158G>A
XM_005264175.3:c.629G>A	XP_005264232.1:p.Trp210Ter
XM_005264175.5:c.629G>A	XP_005264232.1:p.Trp210Ter
XM_006711957.2:c.629G>A	XP_006712020.1:p.Trp210Ter
XM_006711958.2:c.185G>A	XP_006712021.1:p.Trp62Ter
XM_011532662.1:c.482G>A	XP_011530964.1:p.Trp161Ter
XM_011532662.2:c.482G>A	XP_011530964.1:p.Trp161Ter
XM_011532663.1:c.464G>A	XP_011530965.1:p.Trp155Ter
XM_011532663.2:c.464G>A	XP_011530965.1:p.Trp155Ter
XM_011532664.1:c.629G>A	XP_011530966.1:p.Trp210Ter
XM_011532664.2:c.629G>A	XP_011530966.1:p.Trp210Ter
XM_011532668.1:c.629G>A	XP_011530970.1:p.Trp210Ter
XM_017003526.1:c.629G>A	XP_016859015.1:p.Trp210Ter
XR_001738657.1:n.906G>A