Canonical Allele Identifier: CA339184700

Gene: ARID1A

Linked Data

• dbSNP Id: rs2081166554
• gnomAD v4: 1-26779210-C-T
• MyVariant Identifiers: chr1:g.27105701C>T (hg19) ; chr1:g.26779210C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779210C>T , CM000663.2:g.26779210C>T	GRCh38
NC_000001.10:g.27105701C>T , CM000663.1:g.27105701C>T	GRCh37
NC_000001.9:g.26978288C>T	NCBI36
NG_029965.1:g.88180C>T , LRG_875:g.88180C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5312C>T MANE Select	ENSP00000320485.7:p.Pro1771Leu
ENST00000374152.7:c.4163C>T	ENSP00000363267.2:p.Pro1388Leu
ENST00000430799.7:c.4160C>T	ENSP00000390317.3:p.Pro1387Leu
ENST00000466382.2:c.729C>T
ENST00000636219.1:c.4166C>T	ENSP00000489842.1:p.Pro1389Leu
ENST00000637788.1:n.1112C>T
ENST00000324856.11:c.5312C>T	ENSP00000320485.7:p.Pro1771Leu
ENST00000374152.6:c.4163C>T	ENSP00000363267.2:p.Pro1388Leu
ENST00000430799.6:c.2001C>T
ENST00000457599.6:c.4661C>T	ENSP00000387636.2:p.Pro1554Leu
ENST00000466382.1:c.729C>T
ENST00000532781.1:c.810C>T
NM_006015.4:c.5312C>T , LRG_875t1:c.5312C>T	NP_006006.3:p.Pro1771Leu
NM_139135.2:c.4661C>T	NP_624361.1:p.Pro1554Leu
NM_006015.5:c.5312C>T	NP_006006.3:p.Pro1771Leu
NM_139135.3:c.4661C>T	NP_624361.1:p.Pro1554Leu
NM_006015.6:c.5312C>T MANE Select	NP_006006.3:p.Pro1771Leu
NM_139135.4:c.4661C>T	NP_624361.1:p.Pro1554Leu