Canonical Allele Identifier: CA346071685

Gene: DNMT3A

Linked Data

• MyVariant Identifiers: chr2:g.25467041T>G (hg19) ; chr2:g.25244172T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244172T>G , CM000664.2:g.25244172T>G	GRCh38
NC_000002.11:g.25467041T>G , CM000664.1:g.25467041T>G	GRCh37
NC_000002.10:g.25320545T>G	NCBI36
NG_029465.2:g.103419A>C , LRG_459:g.103419A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.153A>C
ENST00000683393.1:c.980A>C	ENSP00000508654.1:n.980A>C
ENST00000683760.1:c.1165A>C	ENSP00000507765.1:p.Asn389His
ENST00000321117.10:c.1834A>C MANE Select	ENSP00000324375.5:p.Asn612His
ENST00000264709.7:c.1834A>C	ENSP00000264709.3:p.Asn612His
ENST00000321117.9:c.1834A>C	ENSP00000324375.5:p.Asn612His
ENST00000380746.8:c.1267A>C	ENSP00000370122.4:p.Asn423His
ENST00000380756.7:c.1834A>C	ENSP00000370132.3:p.Asn612His
ENST00000402667.1:c.1165A>C	ENSP00000384237.1:p.Asn389His
ENST00000474887.5:n.153A>C
NM_022552.4:c.1834A>C , LRG_459t1:c.1834A>C	NP_072046.2:p.Asn612His
NM_153759.3:c.1267A>C , LRG_459t2:c.1267A>C	NP_715640.2:p.Asn423His
NM_175629.2:c.1834A>C , LRG_459t4:c.1834A>C	NP_783328.1:p.Asn612His
XM_005264175.3:c.1834A>C	XP_005264232.1:p.Asn612His
XM_005264177.3:c.1165A>C	XP_005264234.1:p.Asn389His
XM_006711957.2:c.1834A>C	XP_006712020.1:p.Asn612His
XM_006711958.2:c.1390A>C	XP_006712021.1:p.Asn464His
XM_011532662.1:c.1687A>C	XP_011530964.1:p.Asn563His
XM_011532663.1:c.1669A>C	XP_011530965.1:p.Asn557His
XM_011532664.1:c.1834A>C	XP_011530966.1:p.Asn612His
XM_011532665.1:c.1378A>C	XP_011530967.1:p.Asn460His
XM_011532666.1:c.1306A>C	XP_011530968.1:p.Asn436His
XM_011532667.1:c.1165A>C	XP_011530969.1:p.Asn389His
XM_011532668.1:c.1834A>C	XP_011530970.1:p.Asn612His
NM_001320893.1:c.1378A>C	NP_001307822.1:p.Asn460His
NR_135490.1:n.2172A>C
XM_005264175.5:c.1834A>C	XP_005264232.1:p.Asn612His
XM_005264177.4:c.1165A>C	XP_005264234.1:p.Asn389His
XM_011532662.2:c.1687A>C	XP_011530964.1:p.Asn563His
XM_011532663.2:c.1669A>C	XP_011530965.1:p.Asn557His
XM_011532664.2:c.1834A>C	XP_011530966.1:p.Asn612His
XM_011532666.2:c.1306A>C	XP_011530968.1:p.Asn436His
XM_011532667.3:c.1165A>C	XP_011530969.1:p.Asn389His
XM_017003526.1:c.1834A>C	XP_016859015.1:p.Asn612His
XM_017003527.1:c.1165A>C	XP_016859016.1:p.Asn389His
XR_001738657.1:n.2111A>C
NM_001375819.1:c.1165A>C	NP_001362748.1:p.Asn389His
NR_135490.2:n.2065A>C
NM_022552.5:c.1834A>C MANE Select	NP_072046.2:p.Asn612His