Canonical Allele Identifier: CA1239254645

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234389C= , CM000664.2:g.25234389C=	GRCh38
NC_000002.11:g.25457258C= , CM000664.1:g.25457258C=	GRCh37
NC_000002.10:g.25310762C=	NCBI36
NG_029465.2:g.113202G= , LRG_459:g.113202G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.878G=
ENST00000683393.1:c.1775G=	ENSP00000508654.1:n.1775G=
ENST00000683760.1:c.1960G=	ENSP00000507765.1:p.Val654=
ENST00000321117.10:c.2629G= MANE Select	ENSP00000324375.5:p.Val877=
ENST00000264709.7:c.2629G=	ENSP00000264709.3:p.Val877=
ENST00000321117.9:c.2629G=	ENSP00000324375.5:p.Val877=
ENST00000380746.8:c.2062G=	ENSP00000370122.4:p.Val688=
ENST00000380756.7:c.*482G=	ENSP00000370132.3:n.*482G=
ENST00000402667.1:c.1960G=	ENSP00000384237.1:p.Val654=
NM_022552.4:c.2629G= , LRG_459t1:c.2629G=	NP_072046.2:p.Val877=
NM_153759.3:c.2062G= , LRG_459t2:c.2062G=	NP_715640.2:p.Val688=
NM_175629.2:c.2629G= , LRG_459t4:c.2629G=	NP_783328.1:p.Val877=
XM_005264175.3:c.2629G=	XP_005264232.1:p.Val877=
XM_005264177.3:c.1960G=	XP_005264234.1:p.Val654=
XM_006711958.2:c.2185G=	XP_006712021.1:p.Val729=
XM_011532662.1:c.2482G=	XP_011530964.1:p.Val828=
XM_011532663.1:c.2464G=	XP_011530965.1:p.Val822=
XM_011532665.1:c.2173G=	XP_011530967.1:p.Val725=
XM_011532666.1:c.2101G=	XP_011530968.1:p.Val701=
XM_011532667.1:c.1960G=	XP_011530969.1:p.Val654=
NM_001320893.1:c.2173G=	NP_001307822.1:p.Val725=
NR_135490.1:n.3166G=
XM_005264175.5:c.2629G=	XP_005264232.1:p.Val877=
XM_005264177.4:c.1960G=	XP_005264234.1:p.Val654=
XM_011532662.2:c.2482G=	XP_011530964.1:p.Val828=
XM_011532663.2:c.2464G=	XP_011530965.1:p.Val822=
XM_011532666.2:c.2101G=	XP_011530968.1:p.Val701=
XM_011532667.3:c.1960G=	XP_011530969.1:p.Val654=
XM_017003526.1:c.2629G=	XP_016859015.1:p.Val877=
XM_017003527.1:c.1960G=	XP_016859016.1:p.Val654=
XR_001738657.1:n.2836G=
NM_001375819.1:c.1960G=	NP_001362748.1:p.Val654=
NR_135490.2:n.3059G=
NM_022552.5:c.2629G= MANE Select	NP_072046.2:p.Val877=