Canonical Allele Identifier: CA43695836

Gene: DNMT3A

Linked Data

• dbSNP Id: rs1043031759
• MyVariant Identifiers: chr2:g.25457107G>A (hg19) ; chr2:g.25234238G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234238G>A , CM000664.2:g.25234238G>A	GRCh38
NC_000002.11:g.25457107G>A , CM000664.1:g.25457107G>A	GRCh37
NC_000002.10:g.25310611G>A	NCBI36
NG_029465.2:g.113353C>T , LRG_459:g.113353C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683393.1:c.1926C>T	ENSP00000508654.1:n.1926C>T
ENST00000683760.1:c.*41C>T	ENSP00000507765.1:n.*41C>T
ENST00000321117.10:c.*41C>T MANE Select	ENSP00000324375.5:n.*41C>T
ENST00000264709.7:c.*41C>T	ENSP00000264709.3:n.*41C>T
ENST00000321117.9:c.*41C>T	ENSP00000324375.5:n.*41C>T
ENST00000380746.8:c.*41C>T	ENSP00000370122.4:n.*41C>T
ENST00000380756.7:c.*633C>T	ENSP00000370132.3:n.*633C>T
ENST00000402667.1:c.*41C>T	ENSP00000384237.1:n.*41C>T
NM_022552.4:c.*41C>T , LRG_459t1:c.*41C>T	NP_072046.2:n.*41C>T
NM_153759.3:c.*41C>T , LRG_459t2:c.*41C>T	NP_715640.2:n.*41C>T
NM_175629.2:c.*41C>T , LRG_459t4:c.*41C>T	NP_783328.1:n.*41C>T
XM_005264175.3:c.*41C>T	XP_005264232.1:n.*41C>T
XM_005264177.3:c.*41C>T	XP_005264234.1:n.*41C>T
XM_006711958.2:c.*41C>T	XP_006712021.1:n.*41C>T
XM_011532662.1:c.*41C>T	XP_011530964.1:n.*41C>T
XM_011532663.1:c.*41C>T	XP_011530965.1:n.*41C>T
XM_011532665.1:c.*41C>T	XP_011530967.1:n.*41C>T
XM_011532666.1:c.*41C>T	XP_011530968.1:n.*41C>T
XM_011532667.1:c.*41C>T	XP_011530969.1:n.*41C>T
NM_001320893.1:c.*41C>T	NP_001307822.1:n.*41C>T
NR_135490.1:n.3317C>T
XM_005264175.5:c.*41C>T	XP_005264232.1:n.*41C>T
XM_005264177.4:c.*41C>T	XP_005264234.1:n.*41C>T
XM_011532662.2:c.*41C>T	XP_011530964.1:n.*41C>T
XM_011532663.2:c.*41C>T	XP_011530965.1:n.*41C>T
XM_011532666.2:c.*41C>T	XP_011530968.1:n.*41C>T
XM_011532667.3:c.*41C>T	XP_011530969.1:n.*41C>T
XM_017003526.1:c.*41C>T	XP_016859015.1:n.*41C>T
XM_017003527.1:c.*41C>T	XP_016859016.1:n.*41C>T
XR_001738657.1:n.2987C>T
NM_001375819.1:c.*41C>T	NP_001362748.1:n.*41C>T
NR_135490.2:n.3210C>T
NM_022552.5:c.*41C>T MANE Select	NP_072046.2:n.*41C>T