Canonical Allele Identifier: CA425180821

Gene: DNMT3A

Linked Data

• MyVariant Identifiers: chr2:g.25457148T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234279T>C , CM000664.2:g.25234279T>C	GRCh38
NC_000002.11:g.25457148T>C , CM000664.1:g.25457148T>C	GRCh37
NC_000002.10:g.25310652T>C	NCBI36
NG_029465.2:g.113312A>G , LRG_459:g.113312A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.988A>G
ENST00000683393.1:c.1885A>G	ENSP00000508654.1:n.1885A>G
ENST00000683760.1:c.2070A>G	ENSP00000507765.1:p.Ter690=
ENST00000321117.10:c.2739A>G MANE Select	ENSP00000324375.5:p.Ter913=
ENST00000264709.7:c.2739A>G	ENSP00000264709.3:p.Ter913=
ENST00000321117.9:c.2739A>G	ENSP00000324375.5:p.Ter913=
ENST00000380746.8:c.2172A>G	ENSP00000370122.4:p.Ter724=
ENST00000380756.7:c.*592A>G	ENSP00000370132.3:n.*592A>G
ENST00000402667.1:c.2070A>G	ENSP00000384237.1:p.Ter690=
NM_022552.4:c.2739A>G , LRG_459t1:c.2739A>G	NP_072046.2:p.Ter913=
NM_153759.3:c.2172A>G , LRG_459t2:c.2172A>G	NP_715640.2:p.Ter724=
NM_175629.2:c.2739A>G , LRG_459t4:c.2739A>G	NP_783328.1:p.Ter913=
XM_005264175.3:c.2739A>G	XP_005264232.1:p.Ter913=
XM_005264177.3:c.2070A>G	XP_005264234.1:p.Ter690=
XM_006711958.2:c.2295A>G	XP_006712021.1:p.Ter765=
XM_011532662.1:c.2592A>G	XP_011530964.1:p.Ter864=
XM_011532663.1:c.2574A>G	XP_011530965.1:p.Ter858=
XM_011532665.1:c.2283A>G	XP_011530967.1:p.Ter761=
XM_011532666.1:c.2211A>G	XP_011530968.1:p.Ter737=
XM_011532667.1:c.2070A>G	XP_011530969.1:p.Ter690=
NM_001320893.1:c.2283A>G	NP_001307822.1:p.Ter761=
NR_135490.1:n.3276A>G
XM_005264175.5:c.2739A>G	XP_005264232.1:p.Ter913=
XM_005264177.4:c.2070A>G	XP_005264234.1:p.Ter690=
XM_011532662.2:c.2592A>G	XP_011530964.1:p.Ter864=
XM_011532663.2:c.2574A>G	XP_011530965.1:p.Ter858=
XM_011532666.2:c.2211A>G	XP_011530968.1:p.Ter737=
XM_011532667.3:c.2070A>G	XP_011530969.1:p.Ter690=
XM_017003526.1:c.2739A>G	XP_016859015.1:p.Ter913=
XM_017003527.1:c.2070A>G	XP_016859016.1:p.Ter690=
XR_001738657.1:n.2946A>G
NM_001375819.1:c.2070A>G	NP_001362748.1:p.Ter690=
NR_135490.2:n.3169A>G
NM_022552.5:c.2739A>G MANE Select	NP_072046.2:p.Ter913=