Canonical Allele Identifier: CA2658168114

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25234326-T-TCCATG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234326_25234327insCCATG , CM000664.2:g.25234326_25234327insCCATG	GRCh38
NC_000002.11:g.25457195_25457196insCCATG , CM000664.1:g.25457195_25457196insCCATG	GRCh37
NC_000002.10:g.25310699_25310700insCCATG	NCBI36
NG_029465.2:g.113264_113265insCATGG , LRG_459:g.113264_113265insCATGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.940_941insCATGG
ENST00000683393.1:c.1837_1838insCATGG	ENSP00000508654.1:n.1837_1838insCATGG
ENST00000683760.1:c.2022_2023insCATGG	ENSP00000507765.1:p.Ile675HisfsTer10
ENST00000321117.10:c.2691_2692insCATGG MANE Select	ENSP00000324375.5:p.Ile898HisfsTer10
ENST00000264709.7:c.2691_2692insCATGG	ENSP00000264709.3:p.Ile898HisfsTer10
ENST00000321117.9:c.2691_2692insCATGG	ENSP00000324375.5:p.Ile898HisfsTer10
ENST00000380746.8:c.2124_2125insCATGG	ENSP00000370122.4:p.Ile709HisfsTer10
ENST00000380756.7:c.*544_*545insCATGG	ENSP00000370132.3:n.*544_*545insCATGG
ENST00000402667.1:c.2022_2023insCATGG	ENSP00000384237.1:p.Ile675HisfsTer10
NM_022552.4:c.2691_2692insCATGG , LRG_459t1:c.2691_2692insCATGG	NP_072046.2:p.Ile898HisfsTer10
NM_153759.3:c.2124_2125insCATGG , LRG_459t2:c.2124_2125insCATGG	NP_715640.2:p.Ile709HisfsTer10
NM_175629.2:c.2691_2692insCATGG , LRG_459t4:c.2691_2692insCATGG	NP_783328.1:p.Ile898HisfsTer10
XM_005264175.3:c.2691_2692insCATGG	XP_005264232.1:p.Ile898HisfsTer10
XM_005264177.3:c.2022_2023insCATGG	XP_005264234.1:p.Ile675HisfsTer10
XM_006711958.2:c.2247_2248insCATGG	XP_006712021.1:p.Ile750HisfsTer10
XM_011532662.1:c.2544_2545insCATGG	XP_011530964.1:p.Ile849HisfsTer10
XM_011532663.1:c.2526_2527insCATGG	XP_011530965.1:p.Ile843HisfsTer10
XM_011532665.1:c.2235_2236insCATGG	XP_011530967.1:p.Ile746HisfsTer10
XM_011532666.1:c.2163_2164insCATGG	XP_011530968.1:p.Ile722HisfsTer10
XM_011532667.1:c.2022_2023insCATGG	XP_011530969.1:p.Ile675HisfsTer10
NM_001320893.1:c.2235_2236insCATGG	NP_001307822.1:p.Ile746HisfsTer10
NR_135490.1:n.3228_3229insCATGG
XM_005264175.5:c.2691_2692insCATGG	XP_005264232.1:p.Ile898HisfsTer10
XM_005264177.4:c.2022_2023insCATGG	XP_005264234.1:p.Ile675HisfsTer10
XM_011532662.2:c.2544_2545insCATGG	XP_011530964.1:p.Ile849HisfsTer10
XM_011532663.2:c.2526_2527insCATGG	XP_011530965.1:p.Ile843HisfsTer10
XM_011532666.2:c.2163_2164insCATGG	XP_011530968.1:p.Ile722HisfsTer10
XM_011532667.3:c.2022_2023insCATGG	XP_011530969.1:p.Ile675HisfsTer10
XM_017003526.1:c.2691_2692insCATGG	XP_016859015.1:p.Ile898HisfsTer10
XM_017003527.1:c.2022_2023insCATGG	XP_016859016.1:p.Ile675HisfsTer10
XR_001738657.1:n.2898_2899insCATGG
NM_001375819.1:c.2022_2023insCATGG	NP_001362748.1:p.Ile675HisfsTer10
NR_135490.2:n.3121_3122insCATGG
NM_022552.5:c.2691_2692insCATGG MANE Select	NP_072046.2:p.Ile898HisfsTer10