Canonical Allele Identifier: CA1239262743

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244189_25244190delinsTG , CM000664.2:g.25244189_25244190delinsTG	GRCh38
NC_000002.11:g.25467058_25467059delinsTG , CM000664.1:g.25467058_25467059delinsTG	GRCh37
NC_000002.10:g.25320562_25320563delinsTG	NCBI36
NG_029465.2:g.103401_103402delinsCA , LRG_459:g.103401_103402delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.135_136delinsCA
ENST00000683393.1:c.962_963delinsCA	ENSP00000508654.1:n.962_963delinsCA
ENST00000683760.1:c.1147_1148delinsCA	ENSP00000507765.1:p.Gln383=
ENST00000321117.10:c.1816_1817delinsCA MANE Select	ENSP00000324375.5:p.Gln606=
ENST00000264709.7:c.1816_1817delinsCA	ENSP00000264709.3:p.Gln606=
ENST00000321117.9:c.1816_1817delinsCA	ENSP00000324375.5:p.Gln606=
ENST00000380746.8:c.1249_1250delinsCA	ENSP00000370122.4:p.Gln417=
ENST00000380756.7:c.1816_1817delinsCA	ENSP00000370132.3:p.Gln606=
ENST00000402667.1:c.1147_1148delinsCA	ENSP00000384237.1:p.Gln383=
ENST00000474887.5:n.135_136delinsCA
NM_022552.4:c.1816_1817delinsCA , LRG_459t1:c.1816_1817delinsCA	NP_072046.2:p.Gln606=
NM_153759.3:c.1249_1250delinsCA , LRG_459t2:c.1249_1250delinsCA	NP_715640.2:p.Gln417=
NM_175629.2:c.1816_1817delinsCA , LRG_459t4:c.1816_1817delinsCA	NP_783328.1:p.Gln606=
XM_005264175.3:c.1816_1817delinsCA	XP_005264232.1:p.Gln606=
XM_005264177.3:c.1147_1148delinsCA	XP_005264234.1:p.Gln383=
XM_006711957.2:c.1816_1817delinsCA	XP_006712020.1:p.Gln606=
XM_006711958.2:c.1372_1373delinsCA	XP_006712021.1:p.Gln458=
XM_011532662.1:c.1669_1670delinsCA	XP_011530964.1:p.Gln557=
XM_011532663.1:c.1651_1652delinsCA	XP_011530965.1:p.Gln551=
XM_011532664.1:c.1816_1817delinsCA	XP_011530966.1:p.Gln606=
XM_011532665.1:c.1360_1361delinsCA	XP_011530967.1:p.Gln454=
XM_011532666.1:c.1288_1289delinsCA	XP_011530968.1:p.Gln430=
XM_011532667.1:c.1147_1148delinsCA	XP_011530969.1:p.Gln383=
XM_011532668.1:c.1816_1817delinsCA	XP_011530970.1:p.Gln606=
NM_001320893.1:c.1360_1361delinsCA	NP_001307822.1:p.Gln454=
NR_135490.1:n.2154_2155delinsCA
XM_005264175.5:c.1816_1817delinsCA	XP_005264232.1:p.Gln606=
XM_005264177.4:c.1147_1148delinsCA	XP_005264234.1:p.Gln383=
XM_011532662.2:c.1669_1670delinsCA	XP_011530964.1:p.Gln557=
XM_011532663.2:c.1651_1652delinsCA	XP_011530965.1:p.Gln551=
XM_011532664.2:c.1816_1817delinsCA	XP_011530966.1:p.Gln606=
XM_011532666.2:c.1288_1289delinsCA	XP_011530968.1:p.Gln430=
XM_011532667.3:c.1147_1148delinsCA	XP_011530969.1:p.Gln383=
XM_017003526.1:c.1816_1817delinsCA	XP_016859015.1:p.Gln606=
XM_017003527.1:c.1147_1148delinsCA	XP_016859016.1:p.Gln383=
XR_001738657.1:n.2093_2094delinsCA
NM_001375819.1:c.1147_1148delinsCA	NP_001362748.1:p.Gln383=
NR_135490.2:n.2047_2048delinsCA
NM_022552.5:c.1816_1817delinsCA MANE Select	NP_072046.2:p.Gln606=