Canonical Allele Identifier: CA1555465

Gene: DNMT3A

Linked Data

• dbSNP Id: rs149095705
• ExAC: 2:25457176 G / T
• gnomAD v2: 2-25457176-G-T
• gnomAD v3: 2-25234307-G-T
• gnomAD v4: 2-25234307-G-T
• MyVariant Identifiers: chr2:g.25457176G>T (hg19) ; chr2:g.25234307G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234307G>T , CM000664.2:g.25234307G>T	GRCh38
NC_000002.11:g.25457176G>T , CM000664.1:g.25457176G>T	GRCh37
NC_000002.10:g.25310680G>T	NCBI36
NG_029465.2:g.113284C>A , LRG_459:g.113284C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.960C>A
ENST00000683393.1:c.1857C>A	ENSP00000508654.1:n.1857C>A
ENST00000683760.1:c.2042C>A	ENSP00000507765.1:p.Pro681Gln
ENST00000321117.10:c.2711C>A MANE Select	ENSP00000324375.5:p.Pro904Gln
ENST00000264709.7:c.2711C>A	ENSP00000264709.3:p.Pro904Gln
ENST00000321117.9:c.2711C>A	ENSP00000324375.5:p.Pro904Gln
ENST00000380746.8:c.2144C>A	ENSP00000370122.4:p.Pro715Gln
ENST00000380756.7:c.*564C>A	ENSP00000370132.3:n.*564C>A
ENST00000402667.1:c.2042C>A	ENSP00000384237.1:p.Pro681Gln
NM_022552.4:c.2711C>A , LRG_459t1:c.2711C>A	NP_072046.2:p.Pro904Gln
NM_153759.3:c.2144C>A , LRG_459t2:c.2144C>A	NP_715640.2:p.Pro715Gln
NM_175629.2:c.2711C>A , LRG_459t4:c.2711C>A	NP_783328.1:p.Pro904Gln
XM_005264175.3:c.2711C>A	XP_005264232.1:p.Pro904Gln
XM_005264177.3:c.2042C>A	XP_005264234.1:p.Pro681Gln
XM_006711958.2:c.2267C>A	XP_006712021.1:p.Pro756Gln
XM_011532662.1:c.2564C>A	XP_011530964.1:p.Pro855Gln
XM_011532663.1:c.2546C>A	XP_011530965.1:p.Pro849Gln
XM_011532665.1:c.2255C>A	XP_011530967.1:p.Pro752Gln
XM_011532666.1:c.2183C>A	XP_011530968.1:p.Pro728Gln
XM_011532667.1:c.2042C>A	XP_011530969.1:p.Pro681Gln
NM_001320893.1:c.2255C>A	NP_001307822.1:p.Pro752Gln
NR_135490.1:n.3248C>A
XM_005264175.5:c.2711C>A	XP_005264232.1:p.Pro904Gln
XM_005264177.4:c.2042C>A	XP_005264234.1:p.Pro681Gln
XM_011532662.2:c.2564C>A	XP_011530964.1:p.Pro855Gln
XM_011532663.2:c.2546C>A	XP_011530965.1:p.Pro849Gln
XM_011532666.2:c.2183C>A	XP_011530968.1:p.Pro728Gln
XM_011532667.3:c.2042C>A	XP_011530969.1:p.Pro681Gln
XM_017003526.1:c.2711C>A	XP_016859015.1:p.Pro904Gln
XM_017003527.1:c.2042C>A	XP_016859016.1:p.Pro681Gln
XR_001738657.1:n.2918C>A
NM_001375819.1:c.2042C>A	NP_001362748.1:p.Pro681Gln
NR_135490.2:n.3141C>A
NM_022552.5:c.2711C>A MANE Select	NP_072046.2:p.Pro904Gln