Canonical Allele Identifier: CA10584015
Community Standard Title: NM_001374828.1(ARID1B):c.3151C>T (p.Gln1051Ter)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157167101C>T , CM000668.2:g.157167101C>T GRCh38
NC_000006.11:g.157488235C>T , CM000668.1:g.157488235C>T GRCh37
NC_000006.10:g.157529927C>T NCBI36
NG_032093.1:g.394172C>T
NG_032093.2:g.394172C>T
NG_066624.1:g.396076C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.3151C>T MANE Select NP_001361757.1:p.Gln1051Ter
ENST00000636930.2:c.3151C>T MANE Select ENSP00000490491.2:p.Gln1051Ter
NM_001346813.1:c.2902C>T NP_001333742.1:p.Gln968Ter
NM_001363725.1:c.652C>T NP_001350654.1:p.Gln218Ter
NM_001363725.2:c.652C>T NP_001350654.1:p.Gln218Ter
NM_001371656.1:c.3190C>T NP_001358585.1:p.Gln1064Ter
NM_001374820.1:c.3190C>T NP_001361749.1:p.Gln1064Ter
NM_017519.2:c.2902C>T NP_059989.2:p.Gln968Ter
NM_017519.3:c.3151C>T NP_059989.3:p.Gln1051Ter
NM_020732.3:c.2941C>T NP_065783.3:p.Gln981Ter
ENST00000319584.10:c.1168C>T ENSP00000313006.6:p.Gln390Ter
ENST00000319584.11:c.1165C>T ENSP00000313006.7:p.Gln389Ter
ENST00000346085.10:c.3190C>T ENSP00000344546.5:p.Gln1064Ter
ENST00000346085.9:c.2941C>T ENSP00000344546.4:p.Gln981Ter
ENST00000350026.10:c.2902C>T ENSP00000055163.7:p.Gln968Ter
ENST00000350026.11:c.3151C>T ENSP00000055163.8:p.Gln1051Ter
ENST00000350026.9:c.2902C>T ENSP00000055163.7:p.Gln968Ter
ENST00000400790.3:c.103C>T ENSP00000383596.3:p.Gln35Ter
ENST00000414678.6:c.1309C>T ENSP00000412835.2:p.Gln437Ter
ENST00000414678.7:c.1309C>T ENSP00000412835.2:p.Gln437Ter
ENST00000414678.8:c.3061C>T ENSP00000412835.3:p.Gln1021Ter
ENST00000478761.3:c.353C>T
ENST00000635849.1:c.472C>T ENSP00000490948.1:p.Gln158Ter
ENST00000635957.1:c.106C>T ENSP00000490385.1:p.Gln36Ter
ENST00000636426.1:n.315C>T
ENST00000637015.1:c.519C>T
ENST00000637015.2:c.3280C>T ENSP00000489729.2:p.Gln1094Ter
ENST00000637568.1:c.433C>T
ENST00000637722.1:n.1087C>T
ENST00000637810.1:c.652C>T ENSP00000489636.1:p.Gln218Ter
ENST00000637904.1:c.652C>T ENSP00000490550.1:p.Gln218Ter
ENST00000647938.1:c.2941C>T ENSP00000498155.1:p.Gln981Ter
XM_005267069.3:c.2902C>T XP_005267126.2:p.Gln968Ter
XM_011535984.1:c.1981C>T XP_011534286.1:p.Gln661Ter
XM_011535984.2:c.3112C>T XP_011534286.2:p.Gln1038Ter
XM_011535985.1:c.1801C>T XP_011534287.1:p.Gln601Ter
XM_011535986.1:c.1561C>T XP_011534288.1:p.Gln521Ter
XM_011535987.1:c.1180C>T XP_011534289.1:p.Gln394Ter
XM_011535988.1:c.43C>T XP_011534290.1:p.Gln15Ter
XM_011535988.3:c.43C>T XP_011534290.1:p.Gln15Ter
XM_017011103.2:c.3013C>T XP_016866592.1:p.Gln1005Ter
XM_017011104.1:c.2983C>T XP_016866593.1:p.Gln995Ter
XM_017011105.2:c.3112C>T XP_016866594.1:p.Gln1038Ter
XM_017011106.2:c.2983C>T XP_016866595.1:p.Gln995Ter
XM_017011107.2:c.2803C>T XP_016866596.1:p.Gln935Ter
XR_002956289.1:n.3195C>T