Canonical Allele Identifier: CA1239288428

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25295601C= , CM000664.2:g.25295601C=	GRCh38
NC_000002.11:g.25518470C= , CM000664.1:g.25518470C=	GRCh37
NC_000002.10:g.25371974C=	NCBI36
NG_029465.2:g.51990G= , LRG_459:g.51990G=

Transcript Alleles

HGVS	Amino-acid Change
NM_022552.5:c.177+4538G= MANE Select	NP_072046.2:n.177+4538G=
ENST00000321117.10:c.177+4538G= MANE Select	ENSP00000324375.5:n.177+4538G=
NM_001320892.1:c.177+4538G=	NP_001307821.1:n.177+4538G=
NM_001320892.2:c.177+4538G=	NP_001307821.1:n.177+4538G=
NM_022552.4:c.177+4538G= , LRG_459t1:c.177+4538G=	NP_072046.2:n.177+4538G=
NM_175629.2:c.177+4538G= , LRG_459t4:c.177+4538G=	NP_783328.1:n.177+4538G=
NM_175630.1:c.177+4538G= , LRG_459t3:c.177+4538G=	NP_783329.1:n.177+4538G=
NR_135490.1:n.515+4538G=
NR_135490.2:n.408+4538G=
ENST00000264709.7:c.177+4538G=	ENSP00000264709.3:n.177+4538G=
ENST00000321117.9:c.177+4538G=	ENSP00000324375.5:n.177+4538G=
ENST00000380756.7:c.177+4538G=	ENSP00000370132.3:n.177+4538G=
ENST00000406659.3:c.177+4538G=	ENSP00000384852.3:n.177+4538G=
XM_005264175.3:c.177+4538G=	XP_005264232.1:n.177+4538G=
XM_005264175.5:c.177+4538G=	XP_005264232.1:n.177+4538G=
XM_006711957.2:c.177+4538G=	XP_006712020.1:n.177+4538G=
XM_011532663.1:c.-92+4538G=	XP_011530965.1:n.-92+4538G=
XM_011532663.2:c.-92+4538G=	XP_011530965.1:n.-92+4538G=
XM_011532664.1:c.177+4538G=	XP_011530966.1:n.177+4538G=
XM_011532664.2:c.177+4538G=	XP_011530966.1:n.177+4538G=
XM_011532668.1:c.177+4538G=	XP_011530970.1:n.177+4538G=
XM_017003526.1:c.177+4538G=	XP_016859015.1:n.177+4538G=
XR_001738657.1:n.454+4538G=