Canonical Allele Identifier: CA2644294103

Gene: ARID1A

Linked Data

• gnomAD v4: 1-26696674-GGCGGCGGGCCCGGCGCGGAGCCGGACCTGAAGAACTCGAACGGGAACGCGGGCCCTAGGCCCGCCCTGAACAATAACCTCACGGAGCCGCCCGGCGGCGGCGGTGGCGGCAGCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696678_26696791del , CM000663.2:g.26696678_26696791del	GRCh38
NC_000001.10:g.27023169_27023282del , CM000663.1:g.27023169_27023282del	GRCh37
NC_000001.9:g.26895756_26895869del	NCBI36
NG_029965.1:g.5648_5761del , LRG_875:g.5648_5761del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.275_388del MANE Select	ENSP00000320485.7:p.Gly92_Ser129del
ENST00000430799.7:c.-13+3061_-13+3174del	ENSP00000390317.3:n.-13+3061_-13+3174del
ENST00000637465.1:c.-13+578_-13+691del	ENSP00000490650.1:n.-13+578_-13+691del
ENST00000324856.11:c.275_388del	ENSP00000320485.7:p.Gly92_Ser129del
ENST00000457599.6:c.275_388del	ENSP00000387636.2:p.Gly92_Ser129del
NM_006015.4:c.275_388del , LRG_875t1:c.275_388del	NP_006006.3:p.Gly92_Ser129del
NM_139135.2:c.275_388del	NP_624361.1:p.Gly92_Ser129del
NM_006015.5:c.275_388del	NP_006006.3:p.Gly92_Ser129del
NM_139135.3:c.275_388del	NP_624361.1:p.Gly92_Ser129del
NM_006015.6:c.275_388del MANE Select	NP_006006.3:p.Gly92_Ser129del
NM_139135.4:c.275_388del	NP_624361.1:p.Gly92_Ser129del