Canonical Allele Identifier: CA346068004

Gene: DNMT3A

Linked Data

• MyVariant Identifiers: chr2:g.25457155C>G (hg19) ; chr2:g.25234286C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234286C>G , CM000664.2:g.25234286C>G	GRCh38
NC_000002.11:g.25457155C>G , CM000664.1:g.25457155C>G	GRCh37
NC_000002.10:g.25310659C>G	NCBI36
NG_029465.2:g.113305G>C , LRG_459:g.113305G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.981G>C
ENST00000683393.1:c.1878G>C	ENSP00000508654.1:n.1878G>C
ENST00000683760.1:c.2063G>C	ENSP00000507765.1:p.Cys688Ser
ENST00000321117.10:c.2732G>C MANE Select	ENSP00000324375.5:p.Cys911Ser
ENST00000264709.7:c.2732G>C	ENSP00000264709.3:p.Cys911Ser
ENST00000321117.9:c.2732G>C	ENSP00000324375.5:p.Cys911Ser
ENST00000380746.8:c.2165G>C	ENSP00000370122.4:p.Cys722Ser
ENST00000380756.7:c.*585G>C	ENSP00000370132.3:n.*585G>C
ENST00000402667.1:c.2063G>C	ENSP00000384237.1:p.Cys688Ser
NM_022552.4:c.2732G>C , LRG_459t1:c.2732G>C	NP_072046.2:p.Cys911Ser
NM_153759.3:c.2165G>C , LRG_459t2:c.2165G>C	NP_715640.2:p.Cys722Ser
NM_175629.2:c.2732G>C , LRG_459t4:c.2732G>C	NP_783328.1:p.Cys911Ser
XM_005264175.3:c.2732G>C	XP_005264232.1:p.Cys911Ser
XM_005264177.3:c.2063G>C	XP_005264234.1:p.Cys688Ser
XM_006711958.2:c.2288G>C	XP_006712021.1:p.Cys763Ser
XM_011532662.1:c.2585G>C	XP_011530964.1:p.Cys862Ser
XM_011532663.1:c.2567G>C	XP_011530965.1:p.Cys856Ser
XM_011532665.1:c.2276G>C	XP_011530967.1:p.Cys759Ser
XM_011532666.1:c.2204G>C	XP_011530968.1:p.Cys735Ser
XM_011532667.1:c.2063G>C	XP_011530969.1:p.Cys688Ser
NM_001320893.1:c.2276G>C	NP_001307822.1:p.Cys759Ser
NR_135490.1:n.3269G>C
XM_005264175.5:c.2732G>C	XP_005264232.1:p.Cys911Ser
XM_005264177.4:c.2063G>C	XP_005264234.1:p.Cys688Ser
XM_011532662.2:c.2585G>C	XP_011530964.1:p.Cys862Ser
XM_011532663.2:c.2567G>C	XP_011530965.1:p.Cys856Ser
XM_011532666.2:c.2204G>C	XP_011530968.1:p.Cys735Ser
XM_011532667.3:c.2063G>C	XP_011530969.1:p.Cys688Ser
XM_017003526.1:c.2732G>C	XP_016859015.1:p.Cys911Ser
XM_017003527.1:c.2063G>C	XP_016859016.1:p.Cys688Ser
XR_001738657.1:n.2939G>C
NM_001375819.1:c.2063G>C	NP_001362748.1:p.Cys688Ser
NR_135490.2:n.3162G>C
NM_022552.5:c.2732G>C MANE Select	NP_072046.2:p.Cys911Ser