Canonical Allele Identifier: CA346067993

Gene: DNMT3A

Linked Data

• MyVariant Identifiers: chr2:g.25457150A>G (hg19) ; chr2:g.25234281A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234281A>G , CM000664.2:g.25234281A>G	GRCh38
NC_000002.11:g.25457150A>G , CM000664.1:g.25457150A>G	GRCh37
NC_000002.10:g.25310654A>G	NCBI36
NG_029465.2:g.113310T>C , LRG_459:g.113310T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.986T>C
ENST00000683393.1:c.1883T>C	ENSP00000508654.1:n.1883T>C
ENST00000683760.1:c.2068T>C	ENSP00000507765.1:p.Ter690Gln
ENST00000321117.10:c.2737T>C MANE Select	ENSP00000324375.5:p.Ter913Gln
ENST00000264709.7:c.2737T>C	ENSP00000264709.3:p.Ter913Gln
ENST00000321117.9:c.2737T>C	ENSP00000324375.5:p.Ter913Gln
ENST00000380746.8:c.2170T>C	ENSP00000370122.4:p.Ter724Gln
ENST00000380756.7:c.*590T>C	ENSP00000370132.3:n.*590T>C
ENST00000402667.1:c.2068T>C	ENSP00000384237.1:p.Ter690Gln
NM_022552.4:c.2737T>C , LRG_459t1:c.2737T>C	NP_072046.2:p.Ter913Gln
NM_153759.3:c.2170T>C , LRG_459t2:c.2170T>C	NP_715640.2:p.Ter724Gln
NM_175629.2:c.2737T>C , LRG_459t4:c.2737T>C	NP_783328.1:p.Ter913Gln
XM_005264175.3:c.2737T>C	XP_005264232.1:p.Ter913Gln
XM_005264177.3:c.2068T>C	XP_005264234.1:p.Ter690Gln
XM_006711958.2:c.2293T>C	XP_006712021.1:p.Ter765Gln
XM_011532662.1:c.2590T>C	XP_011530964.1:p.Ter864Gln
XM_011532663.1:c.2572T>C	XP_011530965.1:p.Ter858Gln
XM_011532665.1:c.2281T>C	XP_011530967.1:p.Ter761Gln
XM_011532666.1:c.2209T>C	XP_011530968.1:p.Ter737Gln
XM_011532667.1:c.2068T>C	XP_011530969.1:p.Ter690Gln
NM_001320893.1:c.2281T>C	NP_001307822.1:p.Ter761Gln
NR_135490.1:n.3274T>C
XM_005264175.5:c.2737T>C	XP_005264232.1:p.Ter913Gln
XM_005264177.4:c.2068T>C	XP_005264234.1:p.Ter690Gln
XM_011532662.2:c.2590T>C	XP_011530964.1:p.Ter864Gln
XM_011532663.2:c.2572T>C	XP_011530965.1:p.Ter858Gln
XM_011532666.2:c.2209T>C	XP_011530968.1:p.Ter737Gln
XM_011532667.3:c.2068T>C	XP_011530969.1:p.Ter690Gln
XM_017003526.1:c.2737T>C	XP_016859015.1:p.Ter913Gln
XM_017003527.1:c.2068T>C	XP_016859016.1:p.Ter690Gln
XR_001738657.1:n.2944T>C
NM_001375819.1:c.2068T>C	NP_001362748.1:p.Ter690Gln
NR_135490.2:n.3167T>C
NM_022552.5:c.2737T>C MANE Select	NP_072046.2:p.Ter913Gln