Canonical Allele Identifier: CA2658168974

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25244301-G-GCCCCACCAAGAGGTCCACACA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244303_25244323dup , CM000664.2:g.25244303_25244323dup	GRCh38
NC_000002.11:g.25467172_25467192dup , CM000664.1:g.25467172_25467192dup	GRCh37
NC_000002.10:g.25320676_25320696dup	NCBI36
NG_029465.2:g.103269_103289dup , LRG_459:g.103269_103289dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000474887.6:c.3_23dup
ENST00000683393.1:c.830_850dup	ENSP00000508654.1:n.830_850dup
ENST00000683760.1:c.1015_1035dup	ENSP00000507765.1:p.Gly345_Pro346insCysVa...
ENST00000321117.10:c.1684_1704dup MANE Select	ENSP00000324375.5:p.Gly568_Pro569insCysVa...
ENST00000264709.7:c.1684_1704dup	ENSP00000264709.3:p.Gly568_Pro569insCysVa...
ENST00000321117.9:c.1684_1704dup	ENSP00000324375.5:p.Gly568_Pro569insCysVa...
ENST00000380746.8:c.1117_1137dup	ENSP00000370122.4:p.Gly379_Pro380insCysVa...
ENST00000380756.7:c.1684_1704dup	ENSP00000370132.3:p.Gly568_Pro569insCysVa...
ENST00000402667.1:c.1015_1035dup	ENSP00000384237.1:p.Gly345_Pro346insCysVa...
ENST00000474887.5:n.3_23dup
NM_022552.4:c.1684_1704dup , LRG_459t1:c.1684_1704dup	NP_072046.2:p.Gly568_Pro569insCysValAspLe...
NM_153759.3:c.1117_1137dup , LRG_459t2:c.1117_1137dup	NP_715640.2:p.Gly379_Pro380insCysValAspLe...
NM_175629.2:c.1684_1704dup , LRG_459t4:c.1684_1704dup	NP_783328.1:p.Gly568_Pro569insCysValAspLe...
XM_005264175.3:c.1684_1704dup	XP_005264232.1:p.Gly568_Pro569insCysValAs...
XM_005264177.3:c.1015_1035dup	XP_005264234.1:p.Gly345_Pro346insCysValAs...
XM_006711957.2:c.1684_1704dup	XP_006712020.1:p.Gly568_Pro569insCysValAs...
XM_006711958.2:c.1240_1260dup	XP_006712021.1:p.Gly420_Pro421insCysValAs...
XM_011532662.1:c.1537_1557dup	XP_011530964.1:p.Gly519_Pro520insCysValAs...
XM_011532663.1:c.1519_1539dup	XP_011530965.1:p.Gly513_Pro514insCysValAs...
XM_011532664.1:c.1684_1704dup	XP_011530966.1:p.Gly568_Pro569insCysValAs...
XM_011532665.1:c.1228_1248dup	XP_011530967.1:p.Gly416_Pro417insCysValAs...
XM_011532666.1:c.1156_1176dup	XP_011530968.1:p.Gly392_Pro393insCysValAs...
XM_011532667.1:c.1015_1035dup	XP_011530969.1:p.Gly345_Pro346insCysValAs...
XM_011532668.1:c.1684_1704dup	XP_011530970.1:p.Gly568_Pro569insCysValAs...
NM_001320893.1:c.1228_1248dup	NP_001307822.1:p.Gly416_Pro417insCysValAs...
NR_135490.1:n.2022_2042dup
XM_005264175.5:c.1684_1704dup	XP_005264232.1:p.Gly568_Pro569insCysValAs...
XM_005264177.4:c.1015_1035dup	XP_005264234.1:p.Gly345_Pro346insCysValAs...
XM_011532662.2:c.1537_1557dup	XP_011530964.1:p.Gly519_Pro520insCysValAs...
XM_011532663.2:c.1519_1539dup	XP_011530965.1:p.Gly513_Pro514insCysValAs...
XM_011532664.2:c.1684_1704dup	XP_011530966.1:p.Gly568_Pro569insCysValAs...
XM_011532666.2:c.1156_1176dup	XP_011530968.1:p.Gly392_Pro393insCysValAs...
XM_011532667.3:c.1015_1035dup	XP_011530969.1:p.Gly345_Pro346insCysValAs...
XM_017003526.1:c.1684_1704dup	XP_016859015.1:p.Gly568_Pro569insCysValAs...
XM_017003527.1:c.1015_1035dup	XP_016859016.1:p.Gly345_Pro346insCysValAs...
XR_001738657.1:n.1961_1981dup
NM_001375819.1:c.1015_1035dup	NP_001362748.1:p.Gly345_Pro346insCysValAs...
NR_135490.2:n.1915_1935dup
NM_022552.5:c.1684_1704dup MANE Select	NP_072046.2:p.Gly568_Pro569insCysValAspLe...