Canonical Allele Identifier: CA1239265156

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240330_25240331delinsTC , CM000664.2:g.25240330_25240331delinsTC	GRCh38
NC_000002.11:g.25463199_25463200delinsTC , CM000664.1:g.25463199_25463200delinsTC	GRCh37
NC_000002.10:g.25316703_25316704delinsTC	NCBI36
NG_029465.2:g.107260_107261delinsGA , LRG_459:g.107260_107261delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.612_613delinsGA
ENST00000683393.1:c.1439_1440delinsGA	ENSP00000508654.1:n.1439_1440delinsGA
ENST00000683760.1:c.1624_1625delinsGA	ENSP00000507765.1:p.Asp542=
ENST00000321117.10:c.2293_2294delinsGA MANE Select	ENSP00000324375.5:p.Asp765=
ENST00000264709.7:c.2293_2294delinsGA	ENSP00000264709.3:p.Asp765=
ENST00000321117.9:c.2293_2294delinsGA	ENSP00000324375.5:p.Asp765=
ENST00000380746.8:c.1726_1727delinsGA	ENSP00000370122.4:p.Asp576=
ENST00000380756.7:c.2293_2294delinsGA	ENSP00000370132.3:p.Asp765=
ENST00000402667.1:c.1624_1625delinsGA	ENSP00000384237.1:p.Asp542=
ENST00000461228.1:n.512_513delinsGA
ENST00000466601.5:n.665_666delinsGA
ENST00000474887.5:n.612_613delinsGA
ENST00000482935.5:n.293_294delinsGA
ENST00000491288.5:n.310+309_310+310delinsGA
NM_022552.4:c.2293_2294delinsGA , LRG_459t1:c.2293_2294delinsGA	NP_072046.2:p.Asp765=
NM_153759.3:c.1726_1727delinsGA , LRG_459t2:c.1726_1727delinsGA	NP_715640.2:p.Asp576=
NM_175629.2:c.2293_2294delinsGA , LRG_459t4:c.2293_2294delinsGA	NP_783328.1:p.Asp765=
XM_005264175.3:c.2293_2294delinsGA	XP_005264232.1:p.Asp765=
XM_005264177.3:c.1624_1625delinsGA	XP_005264234.1:p.Asp542=
XM_006711957.2:c.2293_2294delinsGA	XP_006712020.1:p.Asp765=
XM_006711958.2:c.1849_1850delinsGA	XP_006712021.1:p.Asp617=
XM_011532662.1:c.2146_2147delinsGA	XP_011530964.1:p.Asp716=
XM_011532663.1:c.2128_2129delinsGA	XP_011530965.1:p.Asp710=
XM_011532664.1:c.2293_2294delinsGA	XP_011530966.1:p.Asp765=
XM_011532665.1:c.1837_1838delinsGA	XP_011530967.1:p.Asp613=
XM_011532666.1:c.1765_1766delinsGA	XP_011530968.1:p.Asp589=
XM_011532667.1:c.1624_1625delinsGA	XP_011530969.1:p.Asp542=
XM_011532668.1:c.2293_2294delinsGA	XP_011530970.1:p.Asp765=
NM_001320893.1:c.1837_1838delinsGA	NP_001307822.1:p.Asp613=
NR_135490.1:n.2631_2632delinsGA
XM_005264175.5:c.2293_2294delinsGA	XP_005264232.1:p.Asp765=
XM_005264177.4:c.1624_1625delinsGA	XP_005264234.1:p.Asp542=
XM_011532662.2:c.2146_2147delinsGA	XP_011530964.1:p.Asp716=
XM_011532663.2:c.2128_2129delinsGA	XP_011530965.1:p.Asp710=
XM_011532664.2:c.2293_2294delinsGA	XP_011530966.1:p.Asp765=
XM_011532666.2:c.1765_1766delinsGA	XP_011530968.1:p.Asp589=
XM_011532667.3:c.1624_1625delinsGA	XP_011530969.1:p.Asp542=
XM_017003526.1:c.2293_2294delinsGA	XP_016859015.1:p.Asp765=
XM_017003527.1:c.1624_1625delinsGA	XP_016859016.1:p.Asp542=
XR_001738657.1:n.2570_2571delinsGA
NM_001375819.1:c.1624_1625delinsGA	NP_001362748.1:p.Asp542=
NR_135490.2:n.2524_2525delinsGA
NM_022552.5:c.2293_2294delinsGA MANE Select	NP_072046.2:p.Asp765=