Canonical Allele Identifier: CA767174713

Gene: DNMT3A

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25255584C>G , CM000664.2:g.25255584C>G	GRCh38
NC_000002.11:g.25478453C>G , CM000664.1:g.25478453C>G	GRCh37
NC_000002.10:g.25331957C>G	NCBI36
NG_029465.2:g.92007G>C , LRG_459:g.92007G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321117.10:c.640-7332G>C MANE Select	ENSP00000324375.5:n.640-7332G>C
ENST00000264709.7:c.640-7332G>C	ENSP00000264709.3:n.640-7332G>C
ENST00000321117.9:c.640-7332G>C	ENSP00000324375.5:n.640-7332G>C
ENST00000380756.7:c.640-7332G>C	ENSP00000370132.3:n.640-7332G>C
NM_022552.4:c.640-7332G>C , LRG_459t1:c.640-7332G>C	NP_072046.2:n.640-7332G>C
NM_175629.2:c.640-7332G>C , LRG_459t4:c.640-7332G>C	NP_783328.1:n.640-7332G>C
XM_005264175.3:c.640-7332G>C	XP_005264232.1:n.640-7332G>C
XM_006711957.2:c.640-7332G>C	XP_006712020.1:n.640-7332G>C
XM_006711958.2:c.196-7332G>C	XP_006712021.1:n.196-7332G>C
XM_011532662.1:c.493-7332G>C	XP_011530964.1:n.493-7332G>C
XM_011532663.1:c.475-7332G>C	XP_011530965.1:n.475-7332G>C
XM_011532664.1:c.640-7332G>C	XP_011530966.1:n.640-7332G>C
XM_011532667.1:c.-31+3969G>C	XP_011530969.1:n.-31+3969G>C
XM_011532668.1:c.640-7332G>C	XP_011530970.1:n.640-7332G>C
NR_135490.1:n.978-7332G>C
XM_005264175.5:c.640-7332G>C	XP_005264232.1:n.640-7332G>C
XM_011532662.2:c.493-7332G>C	XP_011530964.1:n.493-7332G>C
XM_011532663.2:c.475-7332G>C	XP_011530965.1:n.475-7332G>C
XM_011532664.2:c.640-7332G>C	XP_011530966.1:n.640-7332G>C
XM_011532667.3:c.-31+3969G>C	XP_011530969.1:n.-31+3969G>C
XM_017003526.1:c.640-7332G>C	XP_016859015.1:n.640-7332G>C
XM_017003527.1:c.-31+297G>C	XP_016859016.1:n.-31+297G>C
XR_001738657.1:n.917-7332G>C
NR_135490.2:n.871-7332G>C
NM_022552.5:c.640-7332G>C MANE Select	NP_072046.2:n.640-7332G>C