Canonical Allele Identifier: CA425180903

Gene: DNMT3A

Linked Data

• MyVariant Identifiers: chr2:g.25457271G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234402G>T , CM000664.2:g.25234402G>T	GRCh38
NC_000002.11:g.25457271G>T , CM000664.1:g.25457271G>T	GRCh37
NC_000002.10:g.25310775G>T	NCBI36
NG_029465.2:g.113189C>A , LRG_459:g.113189C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.865C>A
ENST00000683393.1:c.1762C>A	ENSP00000508654.1:n.1762C>A
ENST00000683760.1:c.1947C>A	ENSP00000507765.1:p.Val649=
ENST00000321117.10:c.2616C>A MANE Select	ENSP00000324375.5:p.Val872=
ENST00000264709.7:c.2616C>A	ENSP00000264709.3:p.Val872=
ENST00000321117.9:c.2616C>A	ENSP00000324375.5:p.Val872=
ENST00000380746.8:c.2049C>A	ENSP00000370122.4:p.Val683=
ENST00000380756.7:c.*469C>A	ENSP00000370132.3:n.*469C>A
ENST00000402667.1:c.1947C>A	ENSP00000384237.1:p.Val649=
NM_022552.4:c.2616C>A , LRG_459t1:c.2616C>A	NP_072046.2:p.Val872=
NM_153759.3:c.2049C>A , LRG_459t2:c.2049C>A	NP_715640.2:p.Val683=
NM_175629.2:c.2616C>A , LRG_459t4:c.2616C>A	NP_783328.1:p.Val872=
XM_005264175.3:c.2616C>A	XP_005264232.1:p.Val872=
XM_005264177.3:c.1947C>A	XP_005264234.1:p.Val649=
XM_006711958.2:c.2172C>A	XP_006712021.1:p.Val724=
XM_011532662.1:c.2469C>A	XP_011530964.1:p.Val823=
XM_011532663.1:c.2451C>A	XP_011530965.1:p.Val817=
XM_011532665.1:c.2160C>A	XP_011530967.1:p.Val720=
XM_011532666.1:c.2088C>A	XP_011530968.1:p.Val696=
XM_011532667.1:c.1947C>A	XP_011530969.1:p.Val649=
NM_001320893.1:c.2160C>A	NP_001307822.1:p.Val720=
NR_135490.1:n.3153C>A
XM_005264175.5:c.2616C>A	XP_005264232.1:p.Val872=
XM_005264177.4:c.1947C>A	XP_005264234.1:p.Val649=
XM_011532662.2:c.2469C>A	XP_011530964.1:p.Val823=
XM_011532663.2:c.2451C>A	XP_011530965.1:p.Val817=
XM_011532666.2:c.2088C>A	XP_011530968.1:p.Val696=
XM_011532667.3:c.1947C>A	XP_011530969.1:p.Val649=
XM_017003526.1:c.2616C>A	XP_016859015.1:p.Val872=
XM_017003527.1:c.1947C>A	XP_016859016.1:p.Val649=
XR_001738657.1:n.2823C>A
NM_001375819.1:c.1947C>A	NP_001362748.1:p.Val649=
NR_135490.2:n.3046C>A
NM_022552.5:c.2616C>A MANE Select	NP_072046.2:p.Val872=