Canonical Allele Identifier: CA425180913

Gene: DNMT3A

Linked Data

• MyVariant Identifiers: chr2:g.25457280A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234411A>C , CM000664.2:g.25234411A>C	GRCh38
NC_000002.11:g.25457280A>C , CM000664.1:g.25457280A>C	GRCh37
NC_000002.10:g.25310784A>C	NCBI36
NG_029465.2:g.113180T>G , LRG_459:g.113180T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.856T>G
ENST00000683393.1:c.1753T>G	ENSP00000508654.1:n.1753T>G
ENST00000683760.1:c.1938T>G	ENSP00000507765.1:p.Gly646=
ENST00000321117.10:c.2607T>G MANE Select	ENSP00000324375.5:p.Gly869=
ENST00000264709.7:c.2607T>G	ENSP00000264709.3:p.Gly869=
ENST00000321117.9:c.2607T>G	ENSP00000324375.5:p.Gly869=
ENST00000380746.8:c.2040T>G	ENSP00000370122.4:p.Gly680=
ENST00000380756.7:c.*460T>G	ENSP00000370132.3:n.*460T>G
ENST00000402667.1:c.1938T>G	ENSP00000384237.1:p.Gly646=
NM_022552.4:c.2607T>G , LRG_459t1:c.2607T>G	NP_072046.2:p.Gly869=
NM_153759.3:c.2040T>G , LRG_459t2:c.2040T>G	NP_715640.2:p.Gly680=
NM_175629.2:c.2607T>G , LRG_459t4:c.2607T>G	NP_783328.1:p.Gly869=
XM_005264175.3:c.2607T>G	XP_005264232.1:p.Gly869=
XM_005264177.3:c.1938T>G	XP_005264234.1:p.Gly646=
XM_006711958.2:c.2163T>G	XP_006712021.1:p.Gly721=
XM_011532662.1:c.2460T>G	XP_011530964.1:p.Gly820=
XM_011532663.1:c.2442T>G	XP_011530965.1:p.Gly814=
XM_011532665.1:c.2151T>G	XP_011530967.1:p.Gly717=
XM_011532666.1:c.2079T>G	XP_011530968.1:p.Gly693=
XM_011532667.1:c.1938T>G	XP_011530969.1:p.Gly646=
NM_001320893.1:c.2151T>G	NP_001307822.1:p.Gly717=
NR_135490.1:n.3144T>G
XM_005264175.5:c.2607T>G	XP_005264232.1:p.Gly869=
XM_005264177.4:c.1938T>G	XP_005264234.1:p.Gly646=
XM_011532662.2:c.2460T>G	XP_011530964.1:p.Gly820=
XM_011532663.2:c.2442T>G	XP_011530965.1:p.Gly814=
XM_011532666.2:c.2079T>G	XP_011530968.1:p.Gly693=
XM_011532667.3:c.1938T>G	XP_011530969.1:p.Gly646=
XM_017003526.1:c.2607T>G	XP_016859015.1:p.Gly869=
XM_017003527.1:c.1938T>G	XP_016859016.1:p.Gly646=
XR_001738657.1:n.2814T>G
NM_001375819.1:c.1938T>G	NP_001362748.1:p.Gly646=
NR_135490.2:n.3037T>G
NM_022552.5:c.2607T>G MANE Select	NP_072046.2:p.Gly869=