Canonical Allele Identifier: CA1239260259

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234310_25234311delinsGC , CM000664.2:g.25234310_25234311delinsGC	GRCh38
NC_000002.11:g.25457179_25457180delinsGC , CM000664.1:g.25457179_25457180delinsGC	GRCh37
NC_000002.10:g.25310683_25310684delinsGC	NCBI36
NG_029465.2:g.113280_113281delinsGC , LRG_459:g.113280_113281delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.956_957delinsGC
ENST00000683393.1:c.1853_1854delinsGC	ENSP00000508654.1:n.1853_1854delinsGC
ENST00000683760.1:c.2038_2039delinsGC	ENSP00000507765.1:p.Ala680=
ENST00000321117.10:c.2707_2708delinsGC MANE Select	ENSP00000324375.5:p.Ala903=
ENST00000264709.7:c.2707_2708delinsGC	ENSP00000264709.3:p.Ala903=
ENST00000321117.9:c.2707_2708delinsGC	ENSP00000324375.5:p.Ala903=
ENST00000380746.8:c.2140_2141delinsGC	ENSP00000370122.4:p.Ala714=
ENST00000380756.7:c.*560_*561delinsGC	ENSP00000370132.3:n.*560_*561delinsGC
ENST00000402667.1:c.2038_2039delinsGC	ENSP00000384237.1:p.Ala680=
NM_022552.4:c.2707_2708delinsGC , LRG_459t1:c.2707_2708delinsGC	NP_072046.2:p.Ala903=
NM_153759.3:c.2140_2141delinsGC , LRG_459t2:c.2140_2141delinsGC	NP_715640.2:p.Ala714=
NM_175629.2:c.2707_2708delinsGC , LRG_459t4:c.2707_2708delinsGC	NP_783328.1:p.Ala903=
XM_005264175.3:c.2707_2708delinsGC	XP_005264232.1:p.Ala903=
XM_005264177.3:c.2038_2039delinsGC	XP_005264234.1:p.Ala680=
XM_006711958.2:c.2263_2264delinsGC	XP_006712021.1:p.Ala755=
XM_011532662.1:c.2560_2561delinsGC	XP_011530964.1:p.Ala854=
XM_011532663.1:c.2542_2543delinsGC	XP_011530965.1:p.Ala848=
XM_011532665.1:c.2251_2252delinsGC	XP_011530967.1:p.Ala751=
XM_011532666.1:c.2179_2180delinsGC	XP_011530968.1:p.Ala727=
XM_011532667.1:c.2038_2039delinsGC	XP_011530969.1:p.Ala680=
NM_001320893.1:c.2251_2252delinsGC	NP_001307822.1:p.Ala751=
NR_135490.1:n.3244_3245delinsGC
XM_005264175.5:c.2707_2708delinsGC	XP_005264232.1:p.Ala903=
XM_005264177.4:c.2038_2039delinsGC	XP_005264234.1:p.Ala680=
XM_011532662.2:c.2560_2561delinsGC	XP_011530964.1:p.Ala854=
XM_011532663.2:c.2542_2543delinsGC	XP_011530965.1:p.Ala848=
XM_011532666.2:c.2179_2180delinsGC	XP_011530968.1:p.Ala727=
XM_011532667.3:c.2038_2039delinsGC	XP_011530969.1:p.Ala680=
XM_017003526.1:c.2707_2708delinsGC	XP_016859015.1:p.Ala903=
XM_017003527.1:c.2038_2039delinsGC	XP_016859016.1:p.Ala680=
XR_001738657.1:n.2914_2915delinsGC
NM_001375819.1:c.2038_2039delinsGC	NP_001362748.1:p.Ala680=
NR_135490.2:n.3137_3138delinsGC
NM_022552.5:c.2707_2708delinsGC MANE Select	NP_072046.2:p.Ala903=