Canonical Allele Identifier: CA2644294135

Gene: ARID1A

Linked Data

• gnomAD v4: 1-26696817-AGCCGCGGCCGCCTTGCCGCCCCCAGCCTACGGCTTCGGGCAACCCTACGGCCGGAGCCCGTCTGCCGTCGCCGCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696830_26696904del , CM000663.2:g.26696830_26696904del	GRCh38
NC_000001.10:g.27023321_27023395del , CM000663.1:g.27023321_27023395del	GRCh37
NC_000001.9:g.26895908_26895982del	NCBI36
NG_029965.1:g.5800_5874del , LRG_875:g.5800_5874del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.427_501del MANE Select	ENSP00000320485.7:p.Leu143_Ala167del
ENST00000430799.7:c.-13+3213_-13+3287del	ENSP00000390317.3:n.-13+3213_-13+3287del
ENST00000637465.1:c.-13+730_-13+804del	ENSP00000490650.1:n.-13+730_-13+804del
ENST00000324856.11:c.427_501del	ENSP00000320485.7:p.Leu143_Ala167del
ENST00000457599.6:c.427_501del	ENSP00000387636.2:p.Leu143_Ala167del
NM_006015.4:c.427_501del , LRG_875t1:c.427_501del	NP_006006.3:p.Leu143_Ala167del
NM_139135.2:c.427_501del	NP_624361.1:p.Leu143_Ala167del
NM_006015.5:c.427_501del	NP_006006.3:p.Leu143_Ala167del
NM_139135.3:c.427_501del	NP_624361.1:p.Leu143_Ala167del
NM_006015.6:c.427_501del MANE Select	NP_006006.3:p.Leu143_Ala167del
NM_139135.4:c.427_501del	NP_624361.1:p.Leu143_Ala167del