Canonical Allele Identifier: CA1239260078

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25233915_25233918delinsCCTT , CM000664.2:g.25233915_25233918delinsCCTT	GRCh38
NC_000002.11:g.25456784_25456787delinsCCTT , CM000664.1:g.25456784_25456787delinsCCTT	GRCh37
NC_000002.10:g.25310288_25310291delinsCCTT	NCBI36
NG_029465.2:g.113673_113676delinsAAGG , LRG_459:g.113673_113676delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683393.1:c.2246_2249delinsAAGG	ENSP00000508654.1:n.2246_2249delinsAAGG
ENST00000683760.1:c.*361_*364delinsAAGG	ENSP00000507765.1:n.*361_*364delinsAAGG
ENST00000321117.10:c.*361_*364delinsAAGG MANE Select	ENSP00000324375.5:n.*361_*364delinsAAGG
ENST00000264709.7:c.*361_*364delinsAAGG	ENSP00000264709.3:n.*361_*364delinsAAGG
ENST00000321117.9:c.*361_*364delinsAAGG	ENSP00000324375.5:n.*361_*364delinsAAGG
ENST00000380746.8:c.*361_*364delinsAAGG	ENSP00000370122.4:n.*361_*364delinsAAGG
ENST00000380756.7:c.*953_*956delinsAAGG	ENSP00000370132.3:n.*953_*956delinsAAGG
NM_022552.4:c.*361_*364delinsAAGG , LRG_459t1:c.*361_*364delinsAAGG	NP_072046.2:n.*361_*364delinsAAGG
NM_153759.3:c.*361_*364delinsAAGG , LRG_459t2:c.*361_*364delinsAAGG	NP_715640.2:n.*361_*364delinsAAGG
NM_175629.2:c.*361_*364delinsAAGG , LRG_459t4:c.*361_*364delinsAAGG	NP_783328.1:n.*361_*364delinsAAGG
XM_005264175.3:c.*361_*364delinsAAGG	XP_005264232.1:n.*361_*364delinsAAGG
XM_005264177.3:c.*361_*364delinsAAGG	XP_005264234.1:n.*361_*364delinsAAGG
XM_006711958.2:c.*361_*364delinsAAGG	XP_006712021.1:n.*361_*364delinsAAGG
XM_011532662.1:c.*361_*364delinsAAGG	XP_011530964.1:n.*361_*364delinsAAGG
XM_011532663.1:c.*361_*364delinsAAGG	XP_011530965.1:n.*361_*364delinsAAGG
XM_011532665.1:c.*361_*364delinsAAGG	XP_011530967.1:n.*361_*364delinsAAGG
XM_011532666.1:c.*361_*364delinsAAGG	XP_011530968.1:n.*361_*364delinsAAGG
XM_011532667.1:c.*361_*364delinsAAGG	XP_011530969.1:n.*361_*364delinsAAGG
NM_001320893.1:c.*361_*364delinsAAGG	NP_001307822.1:n.*361_*364delinsAAGG
NR_135490.1:n.3637_3640delinsAAGG
XM_005264175.5:c.*361_*364delinsAAGG	XP_005264232.1:n.*361_*364delinsAAGG
XM_005264177.4:c.*361_*364delinsAAGG	XP_005264234.1:n.*361_*364delinsAAGG
XM_011532662.2:c.*361_*364delinsAAGG	XP_011530964.1:n.*361_*364delinsAAGG
XM_011532663.2:c.*361_*364delinsAAGG	XP_011530965.1:n.*361_*364delinsAAGG
XM_011532666.2:c.*361_*364delinsAAGG	XP_011530968.1:n.*361_*364delinsAAGG
XM_011532667.3:c.*361_*364delinsAAGG	XP_011530969.1:n.*361_*364delinsAAGG
XM_017003526.1:c.*361_*364delinsAAGG	XP_016859015.1:n.*361_*364delinsAAGG
XM_017003527.1:c.*361_*364delinsAAGG	XP_016859016.1:n.*361_*364delinsAAGG
XR_001738657.1:n.3307_3310delinsAAGG
NM_001375819.1:c.*361_*364delinsAAGG	NP_001362748.1:n.*361_*364delinsAAGG
NR_135490.2:n.3530_3533delinsAAGG
NM_022552.5:c.*361_*364delinsAAGG MANE Select	NP_072046.2:n.*361_*364delinsAAGG