Canonical Allele Identifier: CA44281970

Gene: DNMT3A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25338138T>A , CM000664.2:g.25338138T>A	GRCh38
NC_000002.11:g.25561007T>A , CM000664.1:g.25561007T>A	GRCh37
NC_000002.10:g.25414511T>A	NCBI36
NG_029465.2:g.9453A>T , LRG_459:g.9453A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321117.10:c.-178+3688A>T MANE Select	ENSP00000324375.5:n.-178+3688A>T
ENST00000264709.7:c.-178+4292A>T	ENSP00000264709.3:n.-178+4292A>T
ENST00000321117.9:c.-178+3688A>T	ENSP00000324375.5:n.-178+3688A>T
ENST00000380756.7:c.-178+4292A>T	ENSP00000370132.3:n.-178+4292A>T
ENST00000406659.3:c.-178+4292A>T	ENSP00000384852.3:n.-178+4292A>T
NM_022552.4:c.-178+3688A>T , LRG_459t1:c.-178+3688A>T	NP_072046.2:n.-178+3688A>T
NM_175629.2:c.-178+4292A>T , LRG_459t4:c.-178+4292A>T	NP_783328.1:n.-178+4292A>T
NM_175630.1:c.-178+4292A>T , LRG_459t3:c.-178+4292A>T	NP_783329.1:n.-178+4292A>T
XM_006711957.2:c.-178+3688A>T	XP_006712020.1:n.-178+3688A>T
XM_011532663.1:c.-446+3688A>T	XP_011530965.1:n.-446+3688A>T
XM_011532664.1:c.-178+3688A>T	XP_011530966.1:n.-178+3688A>T
NM_001320892.1:c.-178+3688A>T	NP_001307821.1:n.-178+3688A>T
NR_135490.1:n.161+4292A>T
XM_011532663.2:c.-446+3688A>T	XP_011530965.1:n.-446+3688A>T
XM_011532664.2:c.-178+3688A>T	XP_011530966.1:n.-178+3688A>T
XR_001738657.1:n.100+3688A>T
NM_001320892.2:c.-178+3688A>T	NP_001307821.1:n.-178+3688A>T
NR_135490.2:n.54+4292A>T
NM_022552.5:c.-178+3688A>T MANE Select	NP_072046.2:n.-178+3688A>T