Canonical Allele Identifier: CA1239260241

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234296A= , CM000664.2:g.25234296A=	GRCh38
NC_000002.11:g.25457165A= , CM000664.1:g.25457165A=	GRCh37
NC_000002.10:g.25310669A=	NCBI36
NG_029465.2:g.113295T= , LRG_459:g.113295T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.971T=
ENST00000683393.1:c.1868T=	ENSP00000508654.1:n.1868T=
ENST00000683760.1:c.2053T=	ENSP00000507765.1:p.Tyr685=
ENST00000321117.10:c.2722T= MANE Select	ENSP00000324375.5:p.Tyr908=
ENST00000264709.7:c.2722T=	ENSP00000264709.3:p.Tyr908=
ENST00000321117.9:c.2722T=	ENSP00000324375.5:p.Tyr908=
ENST00000380746.8:c.2155T=	ENSP00000370122.4:p.Tyr719=
ENST00000380756.7:c.*575T=	ENSP00000370132.3:n.*575T=
ENST00000402667.1:c.2053T=	ENSP00000384237.1:p.Tyr685=
NM_022552.4:c.2722T= , LRG_459t1:c.2722T=	NP_072046.2:p.Tyr908=
NM_153759.3:c.2155T= , LRG_459t2:c.2155T=	NP_715640.2:p.Tyr719=
NM_175629.2:c.2722T= , LRG_459t4:c.2722T=	NP_783328.1:p.Tyr908=
XM_005264175.3:c.2722T=	XP_005264232.1:p.Tyr908=
XM_005264177.3:c.2053T=	XP_005264234.1:p.Tyr685=
XM_006711958.2:c.2278T=	XP_006712021.1:p.Tyr760=
XM_011532662.1:c.2575T=	XP_011530964.1:p.Tyr859=
XM_011532663.1:c.2557T=	XP_011530965.1:p.Tyr853=
XM_011532665.1:c.2266T=	XP_011530967.1:p.Tyr756=
XM_011532666.1:c.2194T=	XP_011530968.1:p.Tyr732=
XM_011532667.1:c.2053T=	XP_011530969.1:p.Tyr685=
NM_001320893.1:c.2266T=	NP_001307822.1:p.Tyr756=
NR_135490.1:n.3259T=
XM_005264175.5:c.2722T=	XP_005264232.1:p.Tyr908=
XM_005264177.4:c.2053T=	XP_005264234.1:p.Tyr685=
XM_011532662.2:c.2575T=	XP_011530964.1:p.Tyr859=
XM_011532663.2:c.2557T=	XP_011530965.1:p.Tyr853=
XM_011532666.2:c.2194T=	XP_011530968.1:p.Tyr732=
XM_011532667.3:c.2053T=	XP_011530969.1:p.Tyr685=
XM_017003526.1:c.2722T=	XP_016859015.1:p.Tyr908=
XM_017003527.1:c.2053T=	XP_016859016.1:p.Tyr685=
XR_001738657.1:n.2929T=
NM_001375819.1:c.2053T=	NP_001362748.1:p.Tyr685=
NR_135490.2:n.3152T=
NM_022552.5:c.2722T= MANE Select	NP_072046.2:p.Tyr908=