Canonical Allele Identifier: CA571907171
Community Standard Title: NM_001374828.1(ARID1B):c.1067_1068insGGC (p.Ala357dup)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.156778747_156778748insGGC , CM000668.2:g.156778747_156778748insGGC GRCh38
NC_000006.11:g.157099881_157099882insGGC , CM000668.1:g.157099881_157099882insGGC GRCh37
NC_000006.10:g.157141573_157141574insGGC NCBI36
NG_032093.1:g.5818_5819insGGC
NG_032093.2:g.5818_5819insGGC
NG_066624.1:g.7722_7723insGGC

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.1067_1068insGGC MANE Select NP_001361757.1:p.Ala356_Ala357insAla
ENST00000636930.2:c.1067_1068insGGC MANE Select ENSP00000490491.2:p.Ala356_Ala357insAla
NM_001346813.1:c.818_819insGGC NP_001333742.1:p.Ala273_Ala274insAla
NM_001371656.1:c.1067_1068insGGC NP_001358585.1:p.Ala356_Ala357insAla
NM_001374820.1:c.1067_1068insGGC NP_001361749.1:p.Ala356_Ala357insAla
NM_017519.2:c.818_819insGGC NP_059989.2:p.Ala273_Ala274insAla
NM_017519.3:c.1067_1068insGGC NP_059989.3:p.Ala356_Ala357insAla
NM_020732.3:c.818_819insGGC NP_065783.3:p.Ala273_Ala274insAla
ENST00000346085.10:c.1067_1068insGGC ENSP00000344546.5:p.Ala356_Ala357insAla
ENST00000346085.9:c.818_819insGGC ENSP00000344546.4:p.Ala273_Ala274insAla
ENST00000350026.10:c.818_819insGGC ENSP00000055163.7:p.Ala273_Ala274insAla
ENST00000350026.11:c.1067_1068insGGC ENSP00000055163.8:p.Ala356_Ala357insAla
ENST00000350026.9:c.818_819insGGC ENSP00000055163.7:p.Ala273_Ala274insAla
ENST00000414678.8:c.1067_1068insGGC ENSP00000412835.3:p.Ala356_Ala357insAla
ENST00000637015.2:c.1067_1068insGGC ENSP00000489729.2:p.Ala356_Ala357insAla
ENST00000647938.1:c.818_819insGGC ENSP00000498155.1:p.Ala273_Ala274insAla
ENST00000674298.1:c.807_808insGGC
XM_005267069.3:c.818_819insGGC XP_005267126.2:p.Ala273_Ala274insAla
XM_011535984.2:c.818_819insGGC XP_011534286.2:p.Ala273_Ala274insAla
XM_017011103.2:c.818_819insGGC XP_016866592.1:p.Ala273_Ala274insAla
XM_017011104.1:c.818_819insGGC XP_016866593.1:p.Ala273_Ala274insAla
XM_017011105.2:c.818_819insGGC XP_016866594.1:p.Ala273_Ala274insAla
XM_017011106.2:c.818_819insGGC XP_016866595.1:p.Ala273_Ala274insAla
XM_017011107.2:c.818_819insGGC XP_016866596.1:p.Ala273_Ala274insAla
XR_002956289.1:n.901_902insGGC