Canonical Allele Identifier: CA2695198380
Community Standard Title: NM_001374828.1(ARID1B):c.980_981delinsGT (p.Pro327Arg)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.156778660_156778661delinsGT , CM000668.2:g.156778660_156778661delinsGT GRCh38
NC_000006.11:g.157099794_157099795delinsGT , CM000668.1:g.157099794_157099795delinsGT GRCh37
NC_000006.10:g.157141486_157141487delinsGT NCBI36
NG_032093.1:g.5731_5732delinsGT
NG_032093.2:g.5731_5732delinsGT
NG_066624.1:g.7635_7636delinsGT

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.980_981delinsGT MANE Select NP_001361757.1:p.Pro327Arg
ENST00000636930.2:c.980_981delinsGT MANE Select ENSP00000490491.2:p.Pro327Arg
NM_001346813.1:c.731_732delinsGT NP_001333742.1:p.Pro244Arg
NM_001371656.1:c.980_981delinsGT NP_001358585.1:p.Pro327Arg
NM_001374820.1:c.980_981delinsGT NP_001361749.1:p.Pro327Arg
NM_017519.2:c.731_732delinsGT NP_059989.2:p.Pro244Arg
NM_017519.3:c.980_981delinsGT NP_059989.3:p.Pro327Arg
NM_020732.3:c.731_732delinsGT NP_065783.3:p.Pro244Arg
ENST00000346085.10:c.980_981delinsGT ENSP00000344546.5:p.Pro327Arg
ENST00000346085.9:c.731_732delinsGT ENSP00000344546.4:p.Pro244Arg
ENST00000350026.10:c.731_732delinsGT ENSP00000055163.7:p.Pro244Arg
ENST00000350026.11:c.980_981delinsGT ENSP00000055163.8:p.Pro327Arg
ENST00000350026.9:c.731_732delinsGT ENSP00000055163.7:p.Pro244Arg
ENST00000414678.8:c.980_981delinsGT ENSP00000412835.3:p.Pro327Arg
ENST00000637015.2:c.980_981delinsGT ENSP00000489729.2:p.Pro327Arg
ENST00000647938.1:c.731_732delinsGT ENSP00000498155.1:p.Pro244Arg
ENST00000674298.1:c.720_721delinsGT
XM_005267069.3:c.731_732delinsGT XP_005267126.2:p.Pro244Arg
XM_011535984.2:c.731_732delinsGT XP_011534286.2:p.Pro244Arg
XM_017011103.2:c.731_732delinsGT XP_016866592.1:p.Pro244Arg
XM_017011104.1:c.731_732delinsGT XP_016866593.1:p.Pro244Arg
XM_017011105.2:c.731_732delinsGT XP_016866594.1:p.Pro244Arg
XM_017011106.2:c.731_732delinsGT XP_016866595.1:p.Pro244Arg
XM_017011107.2:c.731_732delinsGT XP_016866596.1:p.Pro244Arg
XR_002956289.1:n.814_815delinsGT