Canonical Allele Identifier: CA1239254680
Gene: DNMT3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25234405_25234406delinsTG , CM000664.2:g.25234405_25234406delinsTG GRCh38
NC_000002.11:g.25457274_25457275delinsTG , CM000664.1:g.25457274_25457275delinsTG GRCh37
NC_000002.10:g.25310778_25310779delinsTG NCBI36
NG_029465.2:g.113185_113186delinsCA , LRG_459:g.113185_113186delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.861_862delinsCA
ENST00000683393.1:c.1758_1759delinsCA ENSP00000508654.1:n.1758_1759delinsCA
ENST00000683760.1:c.1943_1944delinsCA ENSP00000507765.1:p.Pro648=
ENST00000321117.10:c.2612_2613delinsCA MANE Select ENSP00000324375.5:p.Pro871=
ENST00000264709.7:c.2612_2613delinsCA ENSP00000264709.3:p.Pro871=
ENST00000321117.9:c.2612_2613delinsCA ENSP00000324375.5:p.Pro871=
ENST00000380746.8:c.2045_2046delinsCA ENSP00000370122.4:p.Pro682=
ENST00000380756.7:c.*465_*466delinsCA ENSP00000370132.3:n.*465_*466delinsCA
ENST00000402667.1:c.1943_1944delinsCA ENSP00000384237.1:p.Pro648=
NM_022552.4:c.2612_2613delinsCA , LRG_459t1:c.2612_2613delinsCA NP_072046.2:p.Pro871=
NM_153759.3:c.2045_2046delinsCA , LRG_459t2:c.2045_2046delinsCA NP_715640.2:p.Pro682=
NM_175629.2:c.2612_2613delinsCA , LRG_459t4:c.2612_2613delinsCA NP_783328.1:p.Pro871=
XM_005264175.3:c.2612_2613delinsCA XP_005264232.1:p.Pro871=
XM_005264177.3:c.1943_1944delinsCA XP_005264234.1:p.Pro648=
XM_006711958.2:c.2168_2169delinsCA XP_006712021.1:p.Pro723=
XM_011532662.1:c.2465_2466delinsCA XP_011530964.1:p.Pro822=
XM_011532663.1:c.2447_2448delinsCA XP_011530965.1:p.Pro816=
XM_011532665.1:c.2156_2157delinsCA XP_011530967.1:p.Pro719=
XM_011532666.1:c.2084_2085delinsCA XP_011530968.1:p.Pro695=
XM_011532667.1:c.1943_1944delinsCA XP_011530969.1:p.Pro648=
NM_001320893.1:c.2156_2157delinsCA NP_001307822.1:p.Pro719=
NR_135490.1:n.3149_3150delinsCA
XM_005264175.5:c.2612_2613delinsCA XP_005264232.1:p.Pro871=
XM_005264177.4:c.1943_1944delinsCA XP_005264234.1:p.Pro648=
XM_011532662.2:c.2465_2466delinsCA XP_011530964.1:p.Pro822=
XM_011532663.2:c.2447_2448delinsCA XP_011530965.1:p.Pro816=
XM_011532666.2:c.2084_2085delinsCA XP_011530968.1:p.Pro695=
XM_011532667.3:c.1943_1944delinsCA XP_011530969.1:p.Pro648=
XM_017003526.1:c.2612_2613delinsCA XP_016859015.1:p.Pro871=
XM_017003527.1:c.1943_1944delinsCA XP_016859016.1:p.Pro648=
XR_001738657.1:n.2819_2820delinsCA
NM_001375819.1:c.1943_1944delinsCA NP_001362748.1:p.Pro648=
NR_135490.2:n.3042_3043delinsCA
NM_022552.5:c.2612_2613delinsCA MANE Select NP_072046.2:p.Pro871=