Canonical Allele Identifier: CA346071808

Gene: DNMT3A

Linked Data

• dbSNP Id: rs2149289297
• MyVariant Identifiers: chr2:g.25467103G>C (hg19) ; chr2:g.25244234G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244234G>C , CM000664.2:g.25244234G>C	GRCh38
NC_000002.11:g.25467103G>C , CM000664.1:g.25467103G>C	GRCh37
NC_000002.10:g.25320607G>C	NCBI36
NG_029465.2:g.103357C>G , LRG_459:g.103357C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.91C>G
ENST00000683393.1:c.918C>G	ENSP00000508654.1:n.918C>G
ENST00000683760.1:c.1103C>G	ENSP00000507765.1:p.Thr368Ser
ENST00000321117.10:c.1772C>G MANE Select	ENSP00000324375.5:p.Thr591Ser
ENST00000264709.7:c.1772C>G	ENSP00000264709.3:p.Thr591Ser
ENST00000321117.9:c.1772C>G	ENSP00000324375.5:p.Thr591Ser
ENST00000380746.8:c.1205C>G	ENSP00000370122.4:p.Thr402Ser
ENST00000380756.7:c.1772C>G	ENSP00000370132.3:p.Thr591Ser
ENST00000402667.1:c.1103C>G	ENSP00000384237.1:p.Thr368Ser
ENST00000474887.5:n.91C>G
NM_022552.4:c.1772C>G , LRG_459t1:c.1772C>G	NP_072046.2:p.Thr591Ser
NM_153759.3:c.1205C>G , LRG_459t2:c.1205C>G	NP_715640.2:p.Thr402Ser
NM_175629.2:c.1772C>G , LRG_459t4:c.1772C>G	NP_783328.1:p.Thr591Ser
XM_005264175.3:c.1772C>G	XP_005264232.1:p.Thr591Ser
XM_005264177.3:c.1103C>G	XP_005264234.1:p.Thr368Ser
XM_006711957.2:c.1772C>G	XP_006712020.1:p.Thr591Ser
XM_006711958.2:c.1328C>G	XP_006712021.1:p.Thr443Ser
XM_011532662.1:c.1625C>G	XP_011530964.1:p.Thr542Ser
XM_011532663.1:c.1607C>G	XP_011530965.1:p.Thr536Ser
XM_011532664.1:c.1772C>G	XP_011530966.1:p.Thr591Ser
XM_011532665.1:c.1316C>G	XP_011530967.1:p.Thr439Ser
XM_011532666.1:c.1244C>G	XP_011530968.1:p.Thr415Ser
XM_011532667.1:c.1103C>G	XP_011530969.1:p.Thr368Ser
XM_011532668.1:c.1772C>G	XP_011530970.1:p.Thr591Ser
NM_001320893.1:c.1316C>G	NP_001307822.1:p.Thr439Ser
NR_135490.1:n.2110C>G
XM_005264175.5:c.1772C>G	XP_005264232.1:p.Thr591Ser
XM_005264177.4:c.1103C>G	XP_005264234.1:p.Thr368Ser
XM_011532662.2:c.1625C>G	XP_011530964.1:p.Thr542Ser
XM_011532663.2:c.1607C>G	XP_011530965.1:p.Thr536Ser
XM_011532664.2:c.1772C>G	XP_011530966.1:p.Thr591Ser
XM_011532666.2:c.1244C>G	XP_011530968.1:p.Thr415Ser
XM_011532667.3:c.1103C>G	XP_011530969.1:p.Thr368Ser
XM_017003526.1:c.1772C>G	XP_016859015.1:p.Thr591Ser
XM_017003527.1:c.1103C>G	XP_016859016.1:p.Thr368Ser
XR_001738657.1:n.2049C>G
NM_001375819.1:c.1103C>G	NP_001362748.1:p.Thr368Ser
NR_135490.2:n.2003C>G
NM_022552.5:c.1772C>G MANE Select	NP_072046.2:p.Thr591Ser