Canonical Allele Identifier: CA346068207
Gene: DNMT3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25234388A>C , CM000664.2:g.25234388A>C GRCh38
NC_000002.11:g.25457257A>C , CM000664.1:g.25457257A>C GRCh37
NC_000002.10:g.25310761A>C NCBI36
NG_029465.2:g.113203T>G , LRG_459:g.113203T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.879T>G
ENST00000683393.1:c.1776T>G ENSP00000508654.1:n.1776T>G
ENST00000683760.1:c.1961T>G ENSP00000507765.1:p.Val654Gly
ENST00000321117.10:c.2630T>G MANE Select ENSP00000324375.5:p.Val877Gly
ENST00000264709.7:c.2630T>G ENSP00000264709.3:p.Val877Gly
ENST00000321117.9:c.2630T>G ENSP00000324375.5:p.Val877Gly
ENST00000380746.8:c.2063T>G ENSP00000370122.4:p.Val688Gly
ENST00000380756.7:c.*483T>G ENSP00000370132.3:n.*483T>G
ENST00000402667.1:c.1961T>G ENSP00000384237.1:p.Val654Gly
NM_022552.4:c.2630T>G , LRG_459t1:c.2630T>G NP_072046.2:p.Val877Gly
NM_153759.3:c.2063T>G , LRG_459t2:c.2063T>G NP_715640.2:p.Val688Gly
NM_175629.2:c.2630T>G , LRG_459t4:c.2630T>G NP_783328.1:p.Val877Gly
XM_005264175.3:c.2630T>G XP_005264232.1:p.Val877Gly
XM_005264177.3:c.1961T>G XP_005264234.1:p.Val654Gly
XM_006711958.2:c.2186T>G XP_006712021.1:p.Val729Gly
XM_011532662.1:c.2483T>G XP_011530964.1:p.Val828Gly
XM_011532663.1:c.2465T>G XP_011530965.1:p.Val822Gly
XM_011532665.1:c.2174T>G XP_011530967.1:p.Val725Gly
XM_011532666.1:c.2102T>G XP_011530968.1:p.Val701Gly
XM_011532667.1:c.1961T>G XP_011530969.1:p.Val654Gly
NM_001320893.1:c.2174T>G NP_001307822.1:p.Val725Gly
NR_135490.1:n.3167T>G
XM_005264175.5:c.2630T>G XP_005264232.1:p.Val877Gly
XM_005264177.4:c.1961T>G XP_005264234.1:p.Val654Gly
XM_011532662.2:c.2483T>G XP_011530964.1:p.Val828Gly
XM_011532663.2:c.2465T>G XP_011530965.1:p.Val822Gly
XM_011532666.2:c.2102T>G XP_011530968.1:p.Val701Gly
XM_011532667.3:c.1961T>G XP_011530969.1:p.Val654Gly
XM_017003526.1:c.2630T>G XP_016859015.1:p.Val877Gly
XM_017003527.1:c.1961T>G XP_016859016.1:p.Val654Gly
XR_001738657.1:n.2837T>G
NM_001375819.1:c.1961T>G NP_001362748.1:p.Val654Gly
NR_135490.2:n.3060T>G
NM_022552.5:c.2630T>G MANE Select NP_072046.2:p.Val877Gly