Canonical Allele Identifier: CA2644294009

Gene: ARID1A

Linked Data

• gnomAD v4: 1-26696421-CCCCGCCGCCGCCAGCAGCCTGGGCAACCCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696424_26696453del , CM000663.2:g.26696424_26696453del	GRCh38
NC_000001.10:g.27022915_27022944del , CM000663.1:g.27022915_27022944del	GRCh37
NC_000001.9:g.26895502_26895531del	NCBI36
NG_029965.1:g.5394_5423del , LRG_875:g.5394_5423del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.21_50del MANE Select	ENSP00000320485.7:p.Ala8_Pro17del
ENST00000430799.7:c.-13+2807_-13+2836del	ENSP00000390317.3:n.-13+2807_-13+2836del
ENST00000637465.1:c.-13+324_-13+353del	ENSP00000490650.1:n.-13+324_-13+353del
ENST00000324856.11:c.21_50del	ENSP00000320485.7:p.Ala8_Pro17del
ENST00000457599.6:c.21_50del	ENSP00000387636.2:p.Ala8_Pro17del
NM_006015.4:c.21_50del , LRG_875t1:c.21_50del	NP_006006.3:p.Ala8_Pro17del
NM_139135.2:c.21_50del	NP_624361.1:p.Ala8_Pro17del
NM_006015.5:c.21_50del	NP_006006.3:p.Ala8_Pro17del
NM_139135.3:c.21_50del	NP_624361.1:p.Ala8_Pro17del
NM_006015.6:c.21_50del MANE Select	NP_006006.3:p.Ala8_Pro17del
NM_139135.4:c.21_50del	NP_624361.1:p.Ala8_Pro17del