Canonical Allele Identifier: CA2658168522

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25244221-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244222dup , CM000664.2:g.25244222dup	GRCh38
NC_000002.11:g.25467091dup , CM000664.1:g.25467091dup	GRCh37
NC_000002.10:g.25320595dup	NCBI36
NG_029465.2:g.103369dup , LRG_459:g.103369dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000474887.6:c.103dup
ENST00000683393.1:c.930dup	ENSP00000508654.1:n.930dup
ENST00000683760.1:c.1115dup	ENSP00000507765.1:p.Arg373AlafsTer16
ENST00000321117.10:c.1784dup MANE Select	ENSP00000324375.5:p.Arg596AlafsTer16
ENST00000264709.7:c.1784dup	ENSP00000264709.3:p.Arg596AlafsTer16
ENST00000321117.9:c.1784dup	ENSP00000324375.5:p.Arg596AlafsTer16
ENST00000380746.8:c.1217dup	ENSP00000370122.4:p.Arg407AlafsTer16
ENST00000380756.7:c.1784dup	ENSP00000370132.3:p.Arg596AlafsTer16
ENST00000402667.1:c.1115dup	ENSP00000384237.1:p.Arg373AlafsTer16
ENST00000474887.5:n.103dup
NM_022552.4:c.1784dup , LRG_459t1:c.1784dup	NP_072046.2:p.Arg596AlafsTer16
NM_153759.3:c.1217dup , LRG_459t2:c.1217dup	NP_715640.2:p.Arg407AlafsTer16
NM_175629.2:c.1784dup , LRG_459t4:c.1784dup	NP_783328.1:p.Arg596AlafsTer16
XM_005264175.3:c.1784dup	XP_005264232.1:p.Arg596AlafsTer16
XM_005264177.3:c.1115dup	XP_005264234.1:p.Arg373AlafsTer16
XM_006711957.2:c.1784dup	XP_006712020.1:p.Arg596AlafsTer16
XM_006711958.2:c.1340dup	XP_006712021.1:p.Arg448AlafsTer16
XM_011532662.1:c.1637dup	XP_011530964.1:p.Arg547AlafsTer16
XM_011532663.1:c.1619dup	XP_011530965.1:p.Arg541AlafsTer16
XM_011532664.1:c.1784dup	XP_011530966.1:p.Arg596AlafsTer16
XM_011532665.1:c.1328dup	XP_011530967.1:p.Arg444AlafsTer16
XM_011532666.1:c.1256dup	XP_011530968.1:p.Arg420AlafsTer16
XM_011532667.1:c.1115dup	XP_011530969.1:p.Arg373AlafsTer16
XM_011532668.1:c.1784dup	XP_011530970.1:p.Arg596AlafsTer16
NM_001320893.1:c.1328dup	NP_001307822.1:p.Arg444AlafsTer16
NR_135490.1:n.2122dup
XM_005264175.5:c.1784dup	XP_005264232.1:p.Arg596AlafsTer16
XM_005264177.4:c.1115dup	XP_005264234.1:p.Arg373AlafsTer16
XM_011532662.2:c.1637dup	XP_011530964.1:p.Arg547AlafsTer16
XM_011532663.2:c.1619dup	XP_011530965.1:p.Arg541AlafsTer16
XM_011532664.2:c.1784dup	XP_011530966.1:p.Arg596AlafsTer16
XM_011532666.2:c.1256dup	XP_011530968.1:p.Arg420AlafsTer16
XM_011532667.3:c.1115dup	XP_011530969.1:p.Arg373AlafsTer16
XM_017003526.1:c.1784dup	XP_016859015.1:p.Arg596AlafsTer16
XM_017003527.1:c.1115dup	XP_016859016.1:p.Arg373AlafsTer16
XR_001738657.1:n.2061dup
NM_001375819.1:c.1115dup	NP_001362748.1:p.Arg373AlafsTer16
NR_135490.2:n.2015dup
NM_022552.5:c.1784dup MANE Select	NP_072046.2:p.Arg596AlafsTer16