Canonical Allele Identifier: CA43698617

Gene: DNMT3A

Linked Data

• dbSNP Id: rs767983115
• gnomAD v4: 2-25240322-C-G
• MyVariant Identifiers: chr2:g.25463191C>G (hg19) ; chr2:g.25240322C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240322C>G , CM000664.2:g.25240322C>G	GRCh38
NC_000002.11:g.25463191C>G , CM000664.1:g.25463191C>G	GRCh37
NC_000002.10:g.25316695C>G	NCBI36
NG_029465.2:g.107269G>C , LRG_459:g.107269G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.621G>C
ENST00000683393.1:c.1448G>C	ENSP00000508654.1:n.1448G>C
ENST00000683760.1:c.1633G>C	ENSP00000507765.1:p.Asp545His
ENST00000321117.10:c.2302G>C MANE Select	ENSP00000324375.5:p.Asp768His
ENST00000264709.7:c.2302G>C	ENSP00000264709.3:p.Asp768His
ENST00000321117.9:c.2302G>C	ENSP00000324375.5:p.Asp768His
ENST00000380746.8:c.1735G>C	ENSP00000370122.4:p.Asp579His
ENST00000380756.7:c.2302G>C	ENSP00000370132.3:p.Asp768His
ENST00000402667.1:c.1633G>C	ENSP00000384237.1:p.Asp545His
ENST00000461228.1:n.521G>C
ENST00000466601.5:n.674G>C
ENST00000474887.5:n.621G>C
ENST00000482935.5:n.302G>C
ENST00000491288.5:n.310+318G>C
NM_022552.4:c.2302G>C , LRG_459t1:c.2302G>C	NP_072046.2:p.Asp768His
NM_153759.3:c.1735G>C , LRG_459t2:c.1735G>C	NP_715640.2:p.Asp579His
NM_175629.2:c.2302G>C , LRG_459t4:c.2302G>C	NP_783328.1:p.Asp768His
XM_005264175.3:c.2302G>C	XP_005264232.1:p.Asp768His
XM_005264177.3:c.1633G>C	XP_005264234.1:p.Asp545His
XM_006711957.2:c.2302G>C	XP_006712020.1:p.Asp768His
XM_006711958.2:c.1858G>C	XP_006712021.1:p.Asp620His
XM_011532662.1:c.2155G>C	XP_011530964.1:p.Asp719His
XM_011532663.1:c.2137G>C	XP_011530965.1:p.Asp713His
XM_011532664.1:c.2302G>C	XP_011530966.1:p.Asp768His
XM_011532665.1:c.1846G>C	XP_011530967.1:p.Asp616His
XM_011532666.1:c.1774G>C	XP_011530968.1:p.Asp592His
XM_011532667.1:c.1633G>C	XP_011530969.1:p.Asp545His
XM_011532668.1:c.2302G>C	XP_011530970.1:p.Asp768His
NM_001320893.1:c.1846G>C	NP_001307822.1:p.Asp616His
NR_135490.1:n.2640G>C
XM_005264175.5:c.2302G>C	XP_005264232.1:p.Asp768His
XM_005264177.4:c.1633G>C	XP_005264234.1:p.Asp545His
XM_011532662.2:c.2155G>C	XP_011530964.1:p.Asp719His
XM_011532663.2:c.2137G>C	XP_011530965.1:p.Asp713His
XM_011532664.2:c.2302G>C	XP_011530966.1:p.Asp768His
XM_011532666.2:c.1774G>C	XP_011530968.1:p.Asp592His
XM_011532667.3:c.1633G>C	XP_011530969.1:p.Asp545His
XM_017003526.1:c.2302G>C	XP_016859015.1:p.Asp768His
XM_017003527.1:c.1633G>C	XP_016859016.1:p.Asp545His
XR_001738657.1:n.2579G>C
NM_001375819.1:c.1633G>C	NP_001362748.1:p.Asp545His
NR_135490.2:n.2533G>C
NM_022552.5:c.2302G>C MANE Select	NP_072046.2:p.Asp768His