Canonical Allele Identifier: CA346069734

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25240331-C-A
• MyVariant Identifiers: chr2:g.25463200C>A (hg19) ; chr2:g.25240331C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240331C>A , CM000664.2:g.25240331C>A	GRCh38
NC_000002.11:g.25463200C>A , CM000664.1:g.25463200C>A	GRCh37
NC_000002.10:g.25316704C>A	NCBI36
NG_029465.2:g.107260G>T , LRG_459:g.107260G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.612G>T
ENST00000683393.1:c.1439G>T	ENSP00000508654.1:n.1439G>T
ENST00000683760.1:c.1624G>T	ENSP00000507765.1:p.Asp542Tyr
ENST00000321117.10:c.2293G>T MANE Select	ENSP00000324375.5:p.Asp765Tyr
ENST00000264709.7:c.2293G>T	ENSP00000264709.3:p.Asp765Tyr
ENST00000321117.9:c.2293G>T	ENSP00000324375.5:p.Asp765Tyr
ENST00000380746.8:c.1726G>T	ENSP00000370122.4:p.Asp576Tyr
ENST00000380756.7:c.2293G>T	ENSP00000370132.3:p.Asp765Tyr
ENST00000402667.1:c.1624G>T	ENSP00000384237.1:p.Asp542Tyr
ENST00000461228.1:n.512G>T
ENST00000466601.5:n.665G>T
ENST00000474887.5:n.612G>T
ENST00000482935.5:n.293G>T
ENST00000491288.5:n.310+309G>T
NM_022552.4:c.2293G>T , LRG_459t1:c.2293G>T	NP_072046.2:p.Asp765Tyr
NM_153759.3:c.1726G>T , LRG_459t2:c.1726G>T	NP_715640.2:p.Asp576Tyr
NM_175629.2:c.2293G>T , LRG_459t4:c.2293G>T	NP_783328.1:p.Asp765Tyr
XM_005264175.3:c.2293G>T	XP_005264232.1:p.Asp765Tyr
XM_005264177.3:c.1624G>T	XP_005264234.1:p.Asp542Tyr
XM_006711957.2:c.2293G>T	XP_006712020.1:p.Asp765Tyr
XM_006711958.2:c.1849G>T	XP_006712021.1:p.Asp617Tyr
XM_011532662.1:c.2146G>T	XP_011530964.1:p.Asp716Tyr
XM_011532663.1:c.2128G>T	XP_011530965.1:p.Asp710Tyr
XM_011532664.1:c.2293G>T	XP_011530966.1:p.Asp765Tyr
XM_011532665.1:c.1837G>T	XP_011530967.1:p.Asp613Tyr
XM_011532666.1:c.1765G>T	XP_011530968.1:p.Asp589Tyr
XM_011532667.1:c.1624G>T	XP_011530969.1:p.Asp542Tyr
XM_011532668.1:c.2293G>T	XP_011530970.1:p.Asp765Tyr
NM_001320893.1:c.1837G>T	NP_001307822.1:p.Asp613Tyr
NR_135490.1:n.2631G>T
XM_005264175.5:c.2293G>T	XP_005264232.1:p.Asp765Tyr
XM_005264177.4:c.1624G>T	XP_005264234.1:p.Asp542Tyr
XM_011532662.2:c.2146G>T	XP_011530964.1:p.Asp716Tyr
XM_011532663.2:c.2128G>T	XP_011530965.1:p.Asp710Tyr
XM_011532664.2:c.2293G>T	XP_011530966.1:p.Asp765Tyr
XM_011532666.2:c.1765G>T	XP_011530968.1:p.Asp589Tyr
XM_011532667.3:c.1624G>T	XP_011530969.1:p.Asp542Tyr
XM_017003526.1:c.2293G>T	XP_016859015.1:p.Asp765Tyr
XM_017003527.1:c.1624G>T	XP_016859016.1:p.Asp542Tyr
XR_001738657.1:n.2570G>T
NM_001375819.1:c.1624G>T	NP_001362748.1:p.Asp542Tyr
NR_135490.2:n.2524G>T
NM_022552.5:c.2293G>T MANE Select	NP_072046.2:p.Asp765Tyr