Canonical Allele Identifier: CA2658169043

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25244319-CACA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244320_25244322del , CM000664.2:g.25244320_25244322del	GRCh38
NC_000002.11:g.25467189_25467191del , CM000664.1:g.25467189_25467191del	GRCh37
NC_000002.10:g.25320693_25320695del	NCBI36
NG_029465.2:g.103269_103271del , LRG_459:g.103269_103271del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474887.6:c.3_5del
ENST00000683393.1:c.830_832del	ENSP00000508654.1:n.830_832del
ENST00000683760.1:c.1015_1017del	ENSP00000507765.1:p.Cys339del
ENST00000321117.10:c.1684_1686del MANE Select	ENSP00000324375.5:p.Cys562del
ENST00000264709.7:c.1684_1686del	ENSP00000264709.3:p.Cys562del
ENST00000321117.9:c.1684_1686del	ENSP00000324375.5:p.Cys562del
ENST00000380746.8:c.1117_1119del	ENSP00000370122.4:p.Cys373del
ENST00000380756.7:c.1684_1686del	ENSP00000370132.3:p.Cys562del
ENST00000402667.1:c.1015_1017del	ENSP00000384237.1:p.Cys339del
ENST00000474887.5:n.3_5del
NM_022552.4:c.1684_1686del , LRG_459t1:c.1684_1686del	NP_072046.2:p.Cys562del
NM_153759.3:c.1117_1119del , LRG_459t2:c.1117_1119del	NP_715640.2:p.Cys373del
NM_175629.2:c.1684_1686del , LRG_459t4:c.1684_1686del	NP_783328.1:p.Cys562del
XM_005264175.3:c.1684_1686del	XP_005264232.1:p.Cys562del
XM_005264177.3:c.1015_1017del	XP_005264234.1:p.Cys339del
XM_006711957.2:c.1684_1686del	XP_006712020.1:p.Cys562del
XM_006711958.2:c.1240_1242del	XP_006712021.1:p.Cys414del
XM_011532662.1:c.1537_1539del	XP_011530964.1:p.Cys513del
XM_011532663.1:c.1519_1521del	XP_011530965.1:p.Cys507del
XM_011532664.1:c.1684_1686del	XP_011530966.1:p.Cys562del
XM_011532665.1:c.1228_1230del	XP_011530967.1:p.Cys410del
XM_011532666.1:c.1156_1158del	XP_011530968.1:p.Cys386del
XM_011532667.1:c.1015_1017del	XP_011530969.1:p.Cys339del
XM_011532668.1:c.1684_1686del	XP_011530970.1:p.Cys562del
NM_001320893.1:c.1228_1230del	NP_001307822.1:p.Cys410del
NR_135490.1:n.2022_2024del
XM_005264175.5:c.1684_1686del	XP_005264232.1:p.Cys562del
XM_005264177.4:c.1015_1017del	XP_005264234.1:p.Cys339del
XM_011532662.2:c.1537_1539del	XP_011530964.1:p.Cys513del
XM_011532663.2:c.1519_1521del	XP_011530965.1:p.Cys507del
XM_011532664.2:c.1684_1686del	XP_011530966.1:p.Cys562del
XM_011532666.2:c.1156_1158del	XP_011530968.1:p.Cys386del
XM_011532667.3:c.1015_1017del	XP_011530969.1:p.Cys339del
XM_017003526.1:c.1684_1686del	XP_016859015.1:p.Cys562del
XM_017003527.1:c.1015_1017del	XP_016859016.1:p.Cys339del
XR_001738657.1:n.1961_1963del
NM_001375819.1:c.1015_1017del	NP_001362748.1:p.Cys339del
NR_135490.2:n.1915_1917del
NM_022552.5:c.1684_1686del MANE Select	NP_072046.2:p.Cys562del