Canonical Allele Identifier: CA2658168571

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25234436-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234441_25234442del , CM000664.2:g.25234441_25234442del	GRCh38
NC_000002.11:g.25457310_25457311del , CM000664.1:g.25457310_25457311del	GRCh37
NC_000002.10:g.25310814_25310815del	NCBI36
NG_029465.2:g.113153_113154del , LRG_459:g.113153_113154del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.847-18_847-17del
ENST00000683393.1:c.1744-18_1744-17del	ENSP00000508654.1:n.1744-18_1744-17del
ENST00000683760.1:c.1929-18_1929-17del	ENSP00000507765.1:n.1929-18_1929-17del
ENST00000321117.10:c.2598-18_2598-17del MANE Select	ENSP00000324375.5:n.2598-18_2598-17del
ENST00000264709.7:c.2598-18_2598-17del	ENSP00000264709.3:n.2598-18_2598-17del
ENST00000321117.9:c.2598-18_2598-17del	ENSP00000324375.5:n.2598-18_2598-17del
ENST00000380746.8:c.2031-18_2031-17del	ENSP00000370122.4:n.2031-18_2031-17del
ENST00000380756.7:c.*451-18_*451-17del	ENSP00000370132.3:n.*451-18_*451-17del
ENST00000402667.1:c.1929-18_1929-17del	ENSP00000384237.1:n.1929-18_1929-17del
NM_022552.4:c.2598-18_2598-17del , LRG_459t1:c.2598-18_2598-17del	NP_072046.2:n.2598-18_2598-17del
NM_153759.3:c.2031-18_2031-17del , LRG_459t2:c.2031-18_2031-17del	NP_715640.2:n.2031-18_2031-17del
NM_175629.2:c.2598-18_2598-17del , LRG_459t4:c.2598-18_2598-17del	NP_783328.1:n.2598-18_2598-17del
XM_005264175.3:c.2598-18_2598-17del	XP_005264232.1:n.2598-18_2598-17del
XM_005264177.3:c.1929-18_1929-17del	XP_005264234.1:n.1929-18_1929-17del
XM_006711958.2:c.2154-18_2154-17del	XP_006712021.1:n.2154-18_2154-17del
XM_011532662.1:c.2451-18_2451-17del	XP_011530964.1:n.2451-18_2451-17del
XM_011532663.1:c.2433-18_2433-17del	XP_011530965.1:n.2433-18_2433-17del
XM_011532665.1:c.2142-18_2142-17del	XP_011530967.1:n.2142-18_2142-17del
XM_011532666.1:c.2070-18_2070-17del	XP_011530968.1:n.2070-18_2070-17del
XM_011532667.1:c.1929-18_1929-17del	XP_011530969.1:n.1929-18_1929-17del
NM_001320893.1:c.2142-18_2142-17del	NP_001307822.1:n.2142-18_2142-17del
NR_135490.1:n.3135-18_3135-17del
XM_005264175.5:c.2598-18_2598-17del	XP_005264232.1:n.2598-18_2598-17del
XM_005264177.4:c.1929-18_1929-17del	XP_005264234.1:n.1929-18_1929-17del
XM_011532662.2:c.2451-18_2451-17del	XP_011530964.1:n.2451-18_2451-17del
XM_011532663.2:c.2433-18_2433-17del	XP_011530965.1:n.2433-18_2433-17del
XM_011532666.2:c.2070-18_2070-17del	XP_011530968.1:n.2070-18_2070-17del
XM_011532667.3:c.1929-18_1929-17del	XP_011530969.1:n.1929-18_1929-17del
XM_017003526.1:c.2598-18_2598-17del	XP_016859015.1:n.2598-18_2598-17del
XM_017003527.1:c.1929-18_1929-17del	XP_016859016.1:n.1929-18_1929-17del
XR_001738657.1:n.2805-18_2805-17del
NM_001375819.1:c.1929-18_1929-17del	NP_001362748.1:n.1929-18_1929-17del
NR_135490.2:n.3028-18_3028-17del
NM_022552.5:c.2598-18_2598-17del MANE Select	NP_072046.2:n.2598-18_2598-17del