Canonical Allele Identifier: CA2576694301

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244234_25244248del , CM000664.2:g.25244234_25244248del	GRCh38
NC_000002.11:g.25467103_25467117del , CM000664.1:g.25467103_25467117del	GRCh37
NC_000002.10:g.25320607_25320621del	NCBI36
NG_029465.2:g.103344_103358del , LRG_459:g.103344_103358del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.78_92del
ENST00000683393.1:c.905_919del	ENSP00000508654.1:n.905_919del
ENST00000683760.1:c.1090_1104del	ENSP00000507765.1:p.Gly364_Thr368del
ENST00000321117.10:c.1759_1773del MANE Select	ENSP00000324375.5:p.Gly587_Thr591del
ENST00000264709.7:c.1759_1773del	ENSP00000264709.3:p.Gly587_Thr591del
ENST00000321117.9:c.1759_1773del	ENSP00000324375.5:p.Gly587_Thr591del
ENST00000380746.8:c.1192_1206del	ENSP00000370122.4:p.Gly398_Thr402del
ENST00000380756.7:c.1759_1773del	ENSP00000370132.3:p.Gly587_Thr591del
ENST00000402667.1:c.1090_1104del	ENSP00000384237.1:p.Gly364_Thr368del
ENST00000474887.5:n.78_92del
NM_022552.4:c.1759_1773del , LRG_459t1:c.1759_1773del	NP_072046.2:p.Gly587_Thr591del
NM_153759.3:c.1192_1206del , LRG_459t2:c.1192_1206del	NP_715640.2:p.Gly398_Thr402del
NM_175629.2:c.1759_1773del , LRG_459t4:c.1759_1773del	NP_783328.1:p.Gly587_Thr591del
XM_005264175.3:c.1759_1773del	XP_005264232.1:p.Gly587_Thr591del
XM_005264177.3:c.1090_1104del	XP_005264234.1:p.Gly364_Thr368del
XM_006711957.2:c.1759_1773del	XP_006712020.1:p.Gly587_Thr591del
XM_006711958.2:c.1315_1329del	XP_006712021.1:p.Gly439_Thr443del
XM_011532662.1:c.1612_1626del	XP_011530964.1:p.Gly538_Thr542del
XM_011532663.1:c.1594_1608del	XP_011530965.1:p.Gly532_Thr536del
XM_011532664.1:c.1759_1773del	XP_011530966.1:p.Gly587_Thr591del
XM_011532665.1:c.1303_1317del	XP_011530967.1:p.Gly435_Thr439del
XM_011532666.1:c.1231_1245del	XP_011530968.1:p.Gly411_Thr415del
XM_011532667.1:c.1090_1104del	XP_011530969.1:p.Gly364_Thr368del
XM_011532668.1:c.1759_1773del	XP_011530970.1:p.Gly587_Thr591del
NM_001320893.1:c.1303_1317del	NP_001307822.1:p.Gly435_Thr439del
NR_135490.1:n.2097_2111del
XM_005264175.5:c.1759_1773del	XP_005264232.1:p.Gly587_Thr591del
XM_005264177.4:c.1090_1104del	XP_005264234.1:p.Gly364_Thr368del
XM_011532662.2:c.1612_1626del	XP_011530964.1:p.Gly538_Thr542del
XM_011532663.2:c.1594_1608del	XP_011530965.1:p.Gly532_Thr536del
XM_011532664.2:c.1759_1773del	XP_011530966.1:p.Gly587_Thr591del
XM_011532666.2:c.1231_1245del	XP_011530968.1:p.Gly411_Thr415del
XM_011532667.3:c.1090_1104del	XP_011530969.1:p.Gly364_Thr368del
XM_017003526.1:c.1759_1773del	XP_016859015.1:p.Gly587_Thr591del
XM_017003527.1:c.1090_1104del	XP_016859016.1:p.Gly364_Thr368del
XR_001738657.1:n.2036_2050del
NM_001375819.1:c.1090_1104del	NP_001362748.1:p.Gly364_Thr368del
NR_135490.2:n.1990_2004del
NM_022552.5:c.1759_1773del MANE Select	NP_072046.2:p.Gly587_Thr591del