Canonical Allele Identifier: CA425182301

Gene: DNMT3A

Linked Data

• MyVariant Identifiers: chr2:g.25467105A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244236A>C , CM000664.2:g.25244236A>C	GRCh38
NC_000002.11:g.25467105A>C , CM000664.1:g.25467105A>C	GRCh37
NC_000002.10:g.25320609A>C	NCBI36
NG_029465.2:g.103355T>G , LRG_459:g.103355T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474887.6:c.89T>G
ENST00000683393.1:c.916T>G	ENSP00000508654.1:n.916T>G
ENST00000683760.1:c.1101T>G	ENSP00000507765.1:p.Gly367=
ENST00000321117.10:c.1770T>G MANE Select	ENSP00000324375.5:p.Gly590=
ENST00000264709.7:c.1770T>G	ENSP00000264709.3:p.Gly590=
ENST00000321117.9:c.1770T>G	ENSP00000324375.5:p.Gly590=
ENST00000380746.8:c.1203T>G	ENSP00000370122.4:p.Gly401=
ENST00000380756.7:c.1770T>G	ENSP00000370132.3:p.Gly590=
ENST00000402667.1:c.1101T>G	ENSP00000384237.1:p.Gly367=
ENST00000474887.5:n.89T>G
NM_022552.4:c.1770T>G , LRG_459t1:c.1770T>G	NP_072046.2:p.Gly590=
NM_153759.3:c.1203T>G , LRG_459t2:c.1203T>G	NP_715640.2:p.Gly401=
NM_175629.2:c.1770T>G , LRG_459t4:c.1770T>G	NP_783328.1:p.Gly590=
XM_005264175.3:c.1770T>G	XP_005264232.1:p.Gly590=
XM_005264177.3:c.1101T>G	XP_005264234.1:p.Gly367=
XM_006711957.2:c.1770T>G	XP_006712020.1:p.Gly590=
XM_006711958.2:c.1326T>G	XP_006712021.1:p.Gly442=
XM_011532662.1:c.1623T>G	XP_011530964.1:p.Gly541=
XM_011532663.1:c.1605T>G	XP_011530965.1:p.Gly535=
XM_011532664.1:c.1770T>G	XP_011530966.1:p.Gly590=
XM_011532665.1:c.1314T>G	XP_011530967.1:p.Gly438=
XM_011532666.1:c.1242T>G	XP_011530968.1:p.Gly414=
XM_011532667.1:c.1101T>G	XP_011530969.1:p.Gly367=
XM_011532668.1:c.1770T>G	XP_011530970.1:p.Gly590=
NM_001320893.1:c.1314T>G	NP_001307822.1:p.Gly438=
NR_135490.1:n.2108T>G
XM_005264175.5:c.1770T>G	XP_005264232.1:p.Gly590=
XM_005264177.4:c.1101T>G	XP_005264234.1:p.Gly367=
XM_011532662.2:c.1623T>G	XP_011530964.1:p.Gly541=
XM_011532663.2:c.1605T>G	XP_011530965.1:p.Gly535=
XM_011532664.2:c.1770T>G	XP_011530966.1:p.Gly590=
XM_011532666.2:c.1242T>G	XP_011530968.1:p.Gly414=
XM_011532667.3:c.1101T>G	XP_011530969.1:p.Gly367=
XM_017003526.1:c.1770T>G	XP_016859015.1:p.Gly590=
XM_017003527.1:c.1101T>G	XP_016859016.1:p.Gly367=
XR_001738657.1:n.2047T>G
NM_001375819.1:c.1101T>G	NP_001362748.1:p.Gly367=
NR_135490.2:n.2001T>G
NM_022552.5:c.1770T>G MANE Select	NP_072046.2:p.Gly590=