Canonical Allele Identifier: CA767199101

Gene: DNMT3A

Linked Data

• dbSNP Id: rs1209299922
• MyVariant Identifiers: chr2:g.25529577C>A (hg19) ; chr2:g.25306708C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25306708C>A , CM000664.2:g.25306708C>A	GRCh38
NC_000002.11:g.25529577C>A , CM000664.1:g.25529577C>A	GRCh37
NC_000002.10:g.25383081C>A	NCBI36
NG_029465.2:g.40883G>T , LRG_459:g.40883G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000321117.10:c.73-6465G>T MANE Select	ENSP00000324375.5:n.73-6465G>T
ENST00000264709.7:c.73-6465G>T	ENSP00000264709.3:n.73-6465G>T
ENST00000321117.9:c.73-6465G>T	ENSP00000324375.5:n.73-6465G>T
ENST00000380756.7:c.73-6465G>T	ENSP00000370132.3:n.73-6465G>T
ENST00000406659.3:c.73-6465G>T	ENSP00000384852.3:n.73-6465G>T
NM_022552.4:c.73-6465G>T , LRG_459t1:c.73-6465G>T	NP_072046.2:n.73-6465G>T
NM_175629.2:c.73-6465G>T , LRG_459t4:c.73-6465G>T	NP_783328.1:n.73-6465G>T
NM_175630.1:c.73-6465G>T , LRG_459t3:c.73-6465G>T	NP_783329.1:n.73-6465G>T
XM_005264175.3:c.73-6465G>T	XP_005264232.1:n.73-6465G>T
XM_006711957.2:c.73-6465G>T	XP_006712020.1:n.73-6465G>T
XM_011532663.1:c.-196-6465G>T	XP_011530965.1:n.-196-6465G>T
XM_011532664.1:c.73-6465G>T	XP_011530966.1:n.73-6465G>T
XM_011532668.1:c.73-6465G>T	XP_011530970.1:n.73-6465G>T
NM_001320892.1:c.73-6465G>T	NP_001307821.1:n.73-6465G>T
NR_135490.1:n.411-6465G>T
XM_005264175.5:c.73-6465G>T	XP_005264232.1:n.73-6465G>T
XM_011532663.2:c.-196-6465G>T	XP_011530965.1:n.-196-6465G>T
XM_011532664.2:c.73-6465G>T	XP_011530966.1:n.73-6465G>T
XM_017003526.1:c.73-6465G>T	XP_016859015.1:n.73-6465G>T
XR_001738657.1:n.350-6465G>T
NM_001320892.2:c.73-6465G>T	NP_001307821.1:n.73-6465G>T
NR_135490.2:n.304-6465G>T
NM_022552.5:c.73-6465G>T MANE Select	NP_072046.2:n.73-6465G>T