Canonical Allele Identifier: CA425180886

Gene: DNMT3A

Linked Data

• MyVariant Identifiers: chr2:g.25457253G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234384G>T , CM000664.2:g.25234384G>T	GRCh38
NC_000002.11:g.25457253G>T , CM000664.1:g.25457253G>T	GRCh37
NC_000002.10:g.25310757G>T	NCBI36
NG_029465.2:g.113207C>A , LRG_459:g.113207C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.883C>A
ENST00000683393.1:c.1780C>A	ENSP00000508654.1:n.1780C>A
ENST00000683760.1:c.1965C>A	ENSP00000507765.1:p.Ser655=
ENST00000321117.10:c.2634C>A MANE Select	ENSP00000324375.5:p.Ser878=
ENST00000264709.7:c.2634C>A	ENSP00000264709.3:p.Ser878=
ENST00000321117.9:c.2634C>A	ENSP00000324375.5:p.Ser878=
ENST00000380746.8:c.2067C>A	ENSP00000370122.4:p.Ser689=
ENST00000380756.7:c.*487C>A	ENSP00000370132.3:n.*487C>A
ENST00000402667.1:c.1965C>A	ENSP00000384237.1:p.Ser655=
NM_022552.4:c.2634C>A , LRG_459t1:c.2634C>A	NP_072046.2:p.Ser878=
NM_153759.3:c.2067C>A , LRG_459t2:c.2067C>A	NP_715640.2:p.Ser689=
NM_175629.2:c.2634C>A , LRG_459t4:c.2634C>A	NP_783328.1:p.Ser878=
XM_005264175.3:c.2634C>A	XP_005264232.1:p.Ser878=
XM_005264177.3:c.1965C>A	XP_005264234.1:p.Ser655=
XM_006711958.2:c.2190C>A	XP_006712021.1:p.Ser730=
XM_011532662.1:c.2487C>A	XP_011530964.1:p.Ser829=
XM_011532663.1:c.2469C>A	XP_011530965.1:p.Ser823=
XM_011532665.1:c.2178C>A	XP_011530967.1:p.Ser726=
XM_011532666.1:c.2106C>A	XP_011530968.1:p.Ser702=
XM_011532667.1:c.1965C>A	XP_011530969.1:p.Ser655=
NM_001320893.1:c.2178C>A	NP_001307822.1:p.Ser726=
NR_135490.1:n.3171C>A
XM_005264175.5:c.2634C>A	XP_005264232.1:p.Ser878=
XM_005264177.4:c.1965C>A	XP_005264234.1:p.Ser655=
XM_011532662.2:c.2487C>A	XP_011530964.1:p.Ser829=
XM_011532663.2:c.2469C>A	XP_011530965.1:p.Ser823=
XM_011532666.2:c.2106C>A	XP_011530968.1:p.Ser702=
XM_011532667.3:c.1965C>A	XP_011530969.1:p.Ser655=
XM_017003526.1:c.2634C>A	XP_016859015.1:p.Ser878=
XM_017003527.1:c.1965C>A	XP_016859016.1:p.Ser655=
XR_001738657.1:n.2841C>A
NM_001375819.1:c.1965C>A	NP_001362748.1:p.Ser655=
NR_135490.2:n.3064C>A
NM_022552.5:c.2634C>A MANE Select	NP_072046.2:p.Ser878=