Canonical Allele Identifier: CA1239276803

Gene: DNMT3A

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25269598A>T , CM000664.2:g.25269598A>T	GRCh38
NC_000002.11:g.25492467A>T , CM000664.1:g.25492467A>T	GRCh37
NC_000002.10:g.25345971A>T	NCBI36
NG_029465.2:g.77993T>A , LRG_459:g.77993T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321117.10:c.639+5343T>A MANE Select	ENSP00000324375.5:n.639+5343T>A
ENST00000264709.7:c.639+5343T>A	ENSP00000264709.3:n.639+5343T>A
ENST00000321117.9:c.639+5343T>A	ENSP00000324375.5:n.639+5343T>A
ENST00000380756.7:c.639+5343T>A	ENSP00000370132.3:n.639+5343T>A
NM_022552.4:c.639+5343T>A , LRG_459t1:c.639+5343T>A	NP_072046.2:n.639+5343T>A
NM_175629.2:c.639+5343T>A , LRG_459t4:c.639+5343T>A	NP_783328.1:n.639+5343T>A
XM_005264175.3:c.639+5343T>A	XP_005264232.1:n.639+5343T>A
XM_006711957.2:c.639+5343T>A	XP_006712020.1:n.639+5343T>A
XM_006711958.2:c.195+5343T>A	XP_006712021.1:n.195+5343T>A
XM_011532662.1:c.492+5343T>A	XP_011530964.1:n.492+5343T>A
XM_011532663.1:c.474+5343T>A	XP_011530965.1:n.474+5343T>A
XM_011532664.1:c.639+5343T>A	XP_011530966.1:n.639+5343T>A
XM_011532668.1:c.639+5343T>A	XP_011530970.1:n.639+5343T>A
NR_135490.1:n.977+5343T>A
XM_005264175.5:c.639+5343T>A	XP_005264232.1:n.639+5343T>A
XM_011532662.2:c.492+5343T>A	XP_011530964.1:n.492+5343T>A
XM_011532663.2:c.474+5343T>A	XP_011530965.1:n.474+5343T>A
XM_011532664.2:c.639+5343T>A	XP_011530966.1:n.639+5343T>A
XM_017003526.1:c.639+5343T>A	XP_016859015.1:n.639+5343T>A
XR_001738657.1:n.916+5343T>A
NR_135490.2:n.870+5343T>A
NM_022552.5:c.639+5343T>A MANE Select	NP_072046.2:n.639+5343T>A