Canonical Allele Identifier: CA1028525459

Gene: DNMT3A

Linked Data

• dbSNP Id: rs1673132183
• gnomAD v3: 2-25234482-C-CTGT
• gnomAD v4: 2-25234482-C-CTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234482_25234483insTGT , CM000664.2:g.25234482_25234483insTGT	GRCh38
NC_000002.11:g.25457351_25457352insTGT , CM000664.1:g.25457351_25457352insTGT	GRCh37
NC_000002.10:g.25310855_25310856insTGT	NCBI36
NG_029465.2:g.113108_113109insACA , LRG_459:g.113108_113109insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.847-63_847-62insACA
ENST00000683393.1:c.1744-63_1744-62insACA	ENSP00000508654.1:n.1744-63_1744-62insACA
ENST00000683760.1:c.1929-63_1929-62insACA	ENSP00000507765.1:n.1929-63_1929-62insACA
ENST00000321117.10:c.2598-63_2598-62insACA MANE Select	ENSP00000324375.5:n.2598-63_2598-62insACA
ENST00000264709.7:c.2598-63_2598-62insACA	ENSP00000264709.3:n.2598-63_2598-62insACA
ENST00000321117.9:c.2598-63_2598-62insACA	ENSP00000324375.5:n.2598-63_2598-62insACA
ENST00000380746.8:c.2031-63_2031-62insACA	ENSP00000370122.4:n.2031-63_2031-62insACA
ENST00000380756.7:c.*451-63_*451-62insACA	ENSP00000370132.3:n.*451-63_*451-62insACA
ENST00000402667.1:c.1929-63_1929-62insACA	ENSP00000384237.1:n.1929-63_1929-62insACA
NM_022552.4:c.2598-63_2598-62insACA , LRG_459t1:c.2598-63_2598-62insACA	NP_072046.2:n.2598-63_2598-62insACA
NM_153759.3:c.2031-63_2031-62insACA , LRG_459t2:c.2031-63_2031-62insACA	NP_715640.2:n.2031-63_2031-62insACA
NM_175629.2:c.2598-63_2598-62insACA , LRG_459t4:c.2598-63_2598-62insACA	NP_783328.1:n.2598-63_2598-62insACA
XM_005264175.3:c.2598-63_2598-62insACA	XP_005264232.1:n.2598-63_2598-62insACA
XM_005264177.3:c.1929-63_1929-62insACA	XP_005264234.1:n.1929-63_1929-62insACA
XM_006711958.2:c.2154-63_2154-62insACA	XP_006712021.1:n.2154-63_2154-62insACA
XM_011532662.1:c.2451-63_2451-62insACA	XP_011530964.1:n.2451-63_2451-62insACA
XM_011532663.1:c.2433-63_2433-62insACA	XP_011530965.1:n.2433-63_2433-62insACA
XM_011532665.1:c.2142-63_2142-62insACA	XP_011530967.1:n.2142-63_2142-62insACA
XM_011532666.1:c.2070-63_2070-62insACA	XP_011530968.1:n.2070-63_2070-62insACA
XM_011532667.1:c.1929-63_1929-62insACA	XP_011530969.1:n.1929-63_1929-62insACA
NM_001320893.1:c.2142-63_2142-62insACA	NP_001307822.1:n.2142-63_2142-62insACA
NR_135490.1:n.3135-63_3135-62insACA
XM_005264175.5:c.2598-63_2598-62insACA	XP_005264232.1:n.2598-63_2598-62insACA
XM_005264177.4:c.1929-63_1929-62insACA	XP_005264234.1:n.1929-63_1929-62insACA
XM_011532662.2:c.2451-63_2451-62insACA	XP_011530964.1:n.2451-63_2451-62insACA
XM_011532663.2:c.2433-63_2433-62insACA	XP_011530965.1:n.2433-63_2433-62insACA
XM_011532666.2:c.2070-63_2070-62insACA	XP_011530968.1:n.2070-63_2070-62insACA
XM_011532667.3:c.1929-63_1929-62insACA	XP_011530969.1:n.1929-63_1929-62insACA
XM_017003526.1:c.2598-63_2598-62insACA	XP_016859015.1:n.2598-63_2598-62insACA
XM_017003527.1:c.1929-63_1929-62insACA	XP_016859016.1:n.1929-63_1929-62insACA
XR_001738657.1:n.2805-63_2805-62insACA
NM_001375819.1:c.1929-63_1929-62insACA	NP_001362748.1:n.1929-63_1929-62insACA
NR_135490.2:n.3028-63_3028-62insACA
NM_022552.5:c.2598-63_2598-62insACA MANE Select	NP_072046.2:n.2598-63_2598-62insACA