Canonical Allele Identifier: CA1239265185

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240352_25240353delinsCA , CM000664.2:g.25240352_25240353delinsCA	GRCh38
NC_000002.11:g.25463221_25463222delinsCA , CM000664.1:g.25463221_25463222delinsCA	GRCh37
NC_000002.10:g.25316725_25316726delinsCA	NCBI36
NG_029465.2:g.107238_107239delinsTG , LRG_459:g.107238_107239delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.590_591delinsTG
ENST00000683393.1:c.1417_1418delinsTG	ENSP00000508654.1:n.1417_1418delinsTG
ENST00000683760.1:c.1602_1603delinsTG	ENSP00000507765.1:p.Asn534=
ENST00000321117.10:c.2271_2272delinsTG MANE Select	ENSP00000324375.5:p.Asn757=
ENST00000264709.7:c.2271_2272delinsTG	ENSP00000264709.3:p.Asn757=
ENST00000321117.9:c.2271_2272delinsTG	ENSP00000324375.5:p.Asn757=
ENST00000380746.8:c.1704_1705delinsTG	ENSP00000370122.4:p.Asn568=
ENST00000380756.7:c.2271_2272delinsTG	ENSP00000370132.3:p.Asn757=
ENST00000402667.1:c.1602_1603delinsTG	ENSP00000384237.1:p.Asn534=
ENST00000461228.1:n.490_491delinsTG
ENST00000466601.5:n.643_644delinsTG
ENST00000474887.5:n.590_591delinsTG
ENST00000482935.5:n.271_272delinsTG
ENST00000491288.5:n.310+287_310+288delinsTG
NM_022552.4:c.2271_2272delinsTG , LRG_459t1:c.2271_2272delinsTG	NP_072046.2:p.Asn757=
NM_153759.3:c.1704_1705delinsTG , LRG_459t2:c.1704_1705delinsTG	NP_715640.2:p.Asn568=
NM_175629.2:c.2271_2272delinsTG , LRG_459t4:c.2271_2272delinsTG	NP_783328.1:p.Asn757=
XM_005264175.3:c.2271_2272delinsTG	XP_005264232.1:p.Asn757=
XM_005264177.3:c.1602_1603delinsTG	XP_005264234.1:p.Asn534=
XM_006711957.2:c.2271_2272delinsTG	XP_006712020.1:p.Asn757=
XM_006711958.2:c.1827_1828delinsTG	XP_006712021.1:p.Asn609=
XM_011532662.1:c.2124_2125delinsTG	XP_011530964.1:p.Asn708=
XM_011532663.1:c.2106_2107delinsTG	XP_011530965.1:p.Asn702=
XM_011532664.1:c.2271_2272delinsTG	XP_011530966.1:p.Asn757=
XM_011532665.1:c.1815_1816delinsTG	XP_011530967.1:p.Asn605=
XM_011532666.1:c.1743_1744delinsTG	XP_011530968.1:p.Asn581=
XM_011532667.1:c.1602_1603delinsTG	XP_011530969.1:p.Asn534=
XM_011532668.1:c.2271_2272delinsTG	XP_011530970.1:p.Asn757=
NM_001320893.1:c.1815_1816delinsTG	NP_001307822.1:p.Asn605=
NR_135490.1:n.2609_2610delinsTG
XM_005264175.5:c.2271_2272delinsTG	XP_005264232.1:p.Asn757=
XM_005264177.4:c.1602_1603delinsTG	XP_005264234.1:p.Asn534=
XM_011532662.2:c.2124_2125delinsTG	XP_011530964.1:p.Asn708=
XM_011532663.2:c.2106_2107delinsTG	XP_011530965.1:p.Asn702=
XM_011532664.2:c.2271_2272delinsTG	XP_011530966.1:p.Asn757=
XM_011532666.2:c.1743_1744delinsTG	XP_011530968.1:p.Asn581=
XM_011532667.3:c.1602_1603delinsTG	XP_011530969.1:p.Asn534=
XM_017003526.1:c.2271_2272delinsTG	XP_016859015.1:p.Asn757=
XM_017003527.1:c.1602_1603delinsTG	XP_016859016.1:p.Asn534=
XR_001738657.1:n.2548_2549delinsTG
NM_001375819.1:c.1602_1603delinsTG	NP_001362748.1:p.Asn534=
NR_135490.2:n.2502_2503delinsTG
NM_022552.5:c.2271_2272delinsTG MANE Select	NP_072046.2:p.Asn757=