Canonical Allele Identifier: CA1239262880

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244250_25244251delinsAC , CM000664.2:g.25244250_25244251delinsAC	GRCh38
NC_000002.11:g.25467119_25467120delinsAC , CM000664.1:g.25467119_25467120delinsAC	GRCh37
NC_000002.10:g.25320623_25320624delinsAC	NCBI36
NG_029465.2:g.103340_103341delinsGT , LRG_459:g.103340_103341delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.74_75delinsGT
ENST00000683393.1:c.901_902delinsGT	ENSP00000508654.1:n.901_902delinsGT
ENST00000683760.1:c.1086_1087delinsGT	ENSP00000507765.1:p.Met362=
ENST00000321117.10:c.1755_1756delinsGT MANE Select	ENSP00000324375.5:p.Met585=
ENST00000264709.7:c.1755_1756delinsGT	ENSP00000264709.3:p.Met585=
ENST00000321117.9:c.1755_1756delinsGT	ENSP00000324375.5:p.Met585=
ENST00000380746.8:c.1188_1189delinsGT	ENSP00000370122.4:p.Met396=
ENST00000380756.7:c.1755_1756delinsGT	ENSP00000370132.3:p.Met585=
ENST00000402667.1:c.1086_1087delinsGT	ENSP00000384237.1:p.Met362=
ENST00000474887.5:n.74_75delinsGT
NM_022552.4:c.1755_1756delinsGT , LRG_459t1:c.1755_1756delinsGT	NP_072046.2:p.Met585=
NM_153759.3:c.1188_1189delinsGT , LRG_459t2:c.1188_1189delinsGT	NP_715640.2:p.Met396=
NM_175629.2:c.1755_1756delinsGT , LRG_459t4:c.1755_1756delinsGT	NP_783328.1:p.Met585=
XM_005264175.3:c.1755_1756delinsGT	XP_005264232.1:p.Met585=
XM_005264177.3:c.1086_1087delinsGT	XP_005264234.1:p.Met362=
XM_006711957.2:c.1755_1756delinsGT	XP_006712020.1:p.Met585=
XM_006711958.2:c.1311_1312delinsGT	XP_006712021.1:p.Met437=
XM_011532662.1:c.1608_1609delinsGT	XP_011530964.1:p.Met536=
XM_011532663.1:c.1590_1591delinsGT	XP_011530965.1:p.Met530=
XM_011532664.1:c.1755_1756delinsGT	XP_011530966.1:p.Met585=
XM_011532665.1:c.1299_1300delinsGT	XP_011530967.1:p.Met433=
XM_011532666.1:c.1227_1228delinsGT	XP_011530968.1:p.Met409=
XM_011532667.1:c.1086_1087delinsGT	XP_011530969.1:p.Met362=
XM_011532668.1:c.1755_1756delinsGT	XP_011530970.1:p.Met585=
NM_001320893.1:c.1299_1300delinsGT	NP_001307822.1:p.Met433=
NR_135490.1:n.2093_2094delinsGT
XM_005264175.5:c.1755_1756delinsGT	XP_005264232.1:p.Met585=
XM_005264177.4:c.1086_1087delinsGT	XP_005264234.1:p.Met362=
XM_011532662.2:c.1608_1609delinsGT	XP_011530964.1:p.Met536=
XM_011532663.2:c.1590_1591delinsGT	XP_011530965.1:p.Met530=
XM_011532664.2:c.1755_1756delinsGT	XP_011530966.1:p.Met585=
XM_011532666.2:c.1227_1228delinsGT	XP_011530968.1:p.Met409=
XM_011532667.3:c.1086_1087delinsGT	XP_011530969.1:p.Met362=
XM_017003526.1:c.1755_1756delinsGT	XP_016859015.1:p.Met585=
XM_017003527.1:c.1086_1087delinsGT	XP_016859016.1:p.Met362=
XR_001738657.1:n.2032_2033delinsGT
NM_001375819.1:c.1086_1087delinsGT	NP_001362748.1:p.Met362=
NR_135490.2:n.1986_1987delinsGT
NM_022552.5:c.1755_1756delinsGT MANE Select	NP_072046.2:p.Met585=