Canonical Allele Identifier: CA1239265177

Gene: DNMT3A

Linked Data

• dbSNP Id: rs1673837136

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240343_25240369del , CM000664.2:g.25240343_25240369del	GRCh38
NC_000002.11:g.25463212_25463238del , CM000664.1:g.25463212_25463238del	GRCh37
NC_000002.10:g.25316716_25316742del	NCBI36
NG_029465.2:g.107223_107249del , LRG_459:g.107223_107249del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.575_601del
ENST00000683393.1:c.1402_1428del	ENSP00000508654.1:n.1402_1428del
ENST00000683760.1:c.1587_1613del	ENSP00000507765.1:p.Phe529_Met538delinsLeu
ENST00000321117.10:c.2256_2282del MANE Select	ENSP00000324375.5:p.Phe752_Met761delinsLeu
ENST00000264709.7:c.2256_2282del	ENSP00000264709.3:p.Phe752_Met761delinsLeu
ENST00000321117.9:c.2256_2282del	ENSP00000324375.5:p.Phe752_Met761delinsLeu
ENST00000380746.8:c.1689_1715del	ENSP00000370122.4:p.Phe563_Met572delinsLeu
ENST00000380756.7:c.2256_2282del	ENSP00000370132.3:p.Phe752_Met761delinsLeu
ENST00000402667.1:c.1587_1613del	ENSP00000384237.1:p.Phe529_Met538delinsLeu
ENST00000461228.1:n.475_501del
ENST00000466601.5:n.628_654del
ENST00000474887.5:n.575_601del
ENST00000482935.5:n.256_282del
ENST00000491288.5:n.310+272_310+298del
NM_022552.4:c.2256_2282del , LRG_459t1:c.2256_2282del	NP_072046.2:p.Phe752_Met761delinsLeu
NM_153759.3:c.1689_1715del , LRG_459t2:c.1689_1715del	NP_715640.2:p.Phe563_Met572delinsLeu
NM_175629.2:c.2256_2282del , LRG_459t4:c.2256_2282del	NP_783328.1:p.Phe752_Met761delinsLeu
XM_005264175.3:c.2256_2282del	XP_005264232.1:p.Phe752_Met761delinsLeu
XM_005264177.3:c.1587_1613del	XP_005264234.1:p.Phe529_Met538delinsLeu
XM_006711957.2:c.2256_2282del	XP_006712020.1:p.Phe752_Met761delinsLeu
XM_006711958.2:c.1812_1838del	XP_006712021.1:p.Phe604_Met613delinsLeu
XM_011532662.1:c.2109_2135del	XP_011530964.1:p.Phe703_Met712delinsLeu
XM_011532663.1:c.2091_2117del	XP_011530965.1:p.Phe697_Met706delinsLeu
XM_011532664.1:c.2256_2282del	XP_011530966.1:p.Phe752_Met761delinsLeu
XM_011532665.1:c.1800_1826del	XP_011530967.1:p.Phe600_Met609delinsLeu
XM_011532666.1:c.1728_1754del	XP_011530968.1:p.Phe576_Met585delinsLeu
XM_011532667.1:c.1587_1613del	XP_011530969.1:p.Phe529_Met538delinsLeu
XM_011532668.1:c.2256_2282del	XP_011530970.1:p.Phe752_Met761delinsLeu
NM_001320893.1:c.1800_1826del	NP_001307822.1:p.Phe600_Met609delinsLeu
NR_135490.1:n.2594_2620del
XM_005264175.5:c.2256_2282del	XP_005264232.1:p.Phe752_Met761delinsLeu
XM_005264177.4:c.1587_1613del	XP_005264234.1:p.Phe529_Met538delinsLeu
XM_011532662.2:c.2109_2135del	XP_011530964.1:p.Phe703_Met712delinsLeu
XM_011532663.2:c.2091_2117del	XP_011530965.1:p.Phe697_Met706delinsLeu
XM_011532664.2:c.2256_2282del	XP_011530966.1:p.Phe752_Met761delinsLeu
XM_011532666.2:c.1728_1754del	XP_011530968.1:p.Phe576_Met585delinsLeu
XM_011532667.3:c.1587_1613del	XP_011530969.1:p.Phe529_Met538delinsLeu
XM_017003526.1:c.2256_2282del	XP_016859015.1:p.Phe752_Met761delinsLeu
XM_017003527.1:c.1587_1613del	XP_016859016.1:p.Phe529_Met538delinsLeu
XR_001738657.1:n.2533_2559del
NM_001375819.1:c.1587_1613del	NP_001362748.1:p.Phe529_Met538delinsLeu
NR_135490.2:n.2487_2513del
NM_022552.5:c.2256_2282del MANE Select	NP_072046.2:p.Phe752_Met761delinsLeu