Canonical Allele Identifier: CA1239254536

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234360_25234361delinsCT , CM000664.2:g.25234360_25234361delinsCT	GRCh38
NC_000002.11:g.25457229_25457230delinsCT , CM000664.1:g.25457229_25457230delinsCT	GRCh37
NC_000002.10:g.25310733_25310734delinsCT	NCBI36
NG_029465.2:g.113230_113231delinsAG , LRG_459:g.113230_113231delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.906_907delinsAG
ENST00000683393.1:c.1803_1804delinsAG	ENSP00000508654.1:n.1803_1804delinsAG
ENST00000683760.1:c.1988_1989delinsAG	ENSP00000507765.1:p.Gln663=
ENST00000321117.10:c.2657_2658delinsAG MANE Select	ENSP00000324375.5:p.Gln886=
ENST00000264709.7:c.2657_2658delinsAG	ENSP00000264709.3:p.Gln886=
ENST00000321117.9:c.2657_2658delinsAG	ENSP00000324375.5:p.Gln886=
ENST00000380746.8:c.2090_2091delinsAG	ENSP00000370122.4:p.Gln697=
ENST00000380756.7:c.*510_*511delinsAG	ENSP00000370132.3:n.*510_*511delinsAG
ENST00000402667.1:c.1988_1989delinsAG	ENSP00000384237.1:p.Gln663=
NM_022552.4:c.2657_2658delinsAG , LRG_459t1:c.2657_2658delinsAG	NP_072046.2:p.Gln886=
NM_153759.3:c.2090_2091delinsAG , LRG_459t2:c.2090_2091delinsAG	NP_715640.2:p.Gln697=
NM_175629.2:c.2657_2658delinsAG , LRG_459t4:c.2657_2658delinsAG	NP_783328.1:p.Gln886=
XM_005264175.3:c.2657_2658delinsAG	XP_005264232.1:p.Gln886=
XM_005264177.3:c.1988_1989delinsAG	XP_005264234.1:p.Gln663=
XM_006711958.2:c.2213_2214delinsAG	XP_006712021.1:p.Gln738=
XM_011532662.1:c.2510_2511delinsAG	XP_011530964.1:p.Gln837=
XM_011532663.1:c.2492_2493delinsAG	XP_011530965.1:p.Gln831=
XM_011532665.1:c.2201_2202delinsAG	XP_011530967.1:p.Gln734=
XM_011532666.1:c.2129_2130delinsAG	XP_011530968.1:p.Gln710=
XM_011532667.1:c.1988_1989delinsAG	XP_011530969.1:p.Gln663=
NM_001320893.1:c.2201_2202delinsAG	NP_001307822.1:p.Gln734=
NR_135490.1:n.3194_3195delinsAG
XM_005264175.5:c.2657_2658delinsAG	XP_005264232.1:p.Gln886=
XM_005264177.4:c.1988_1989delinsAG	XP_005264234.1:p.Gln663=
XM_011532662.2:c.2510_2511delinsAG	XP_011530964.1:p.Gln837=
XM_011532663.2:c.2492_2493delinsAG	XP_011530965.1:p.Gln831=
XM_011532666.2:c.2129_2130delinsAG	XP_011530968.1:p.Gln710=
XM_011532667.3:c.1988_1989delinsAG	XP_011530969.1:p.Gln663=
XM_017003526.1:c.2657_2658delinsAG	XP_016859015.1:p.Gln886=
XM_017003527.1:c.1988_1989delinsAG	XP_016859016.1:p.Gln663=
XR_001738657.1:n.2864_2865delinsAG
NM_001375819.1:c.1988_1989delinsAG	NP_001362748.1:p.Gln663=
NR_135490.2:n.3087_3088delinsAG
NM_022552.5:c.2657_2658delinsAG MANE Select	NP_072046.2:p.Gln886=