Canonical Allele Identifier: CA2695207237
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157148656dup , CM000668.2:g.157148656dup GRCh38
NC_000006.11:g.157469790dup , CM000668.1:g.157469790dup GRCh37
NC_000006.10:g.157511482dup NCBI36
NG_032093.1:g.375727dup
NG_032093.2:g.375727dup
NG_066624.1:g.377631dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.2794dup ENSP00000055163.8:p.Val932GlyfsTer?
ENST00000414678.8:c.2704dup ENSP00000412835.3:p.Val902GlyfsTer?
ENST00000637015.2:c.2794dup ENSP00000489729.2:p.Val932GlyfsTer?
ENST00000319584.11:c.808dup ENSP00000313006.7:p.Val270GlyfsTer?
ENST00000346085.10:c.2833dup ENSP00000344546.5:p.Val945GlyfsTer?
ENST00000350026.10:c.2545dup ENSP00000055163.7:p.Val849GlyfsTer?
ENST00000414678.7:c.952dup ENSP00000412835.2:p.Val318GlyfsTer?
ENST00000452544.2:n.695dup
ENST00000635849.1:c.115dup ENSP00000490948.1:p.Val39GlyfsTer?
ENST00000636930.2:c.2794dup MANE Select ENSP00000490491.2:p.Val932GlyfsTer?
ENST00000637015.1:c.33dup
ENST00000637810.1:c.295dup ENSP00000489636.1:p.Val99GlyfsTer?
ENST00000637904.1:c.295dup ENSP00000490550.1:p.Val99GlyfsTer?
ENST00000647938.1:c.2584dup ENSP00000498155.1:p.Val862GlyfsTer?
ENST00000674190.1:n.1543dup
ENST00000319584.10:c.811dup ENSP00000313006.6:p.Val271GlyfsTer?
ENST00000346085.9:c.2584dup ENSP00000344546.4:p.Val862GlyfsTer?
ENST00000350026.9:c.2545dup ENSP00000055163.7:p.Val849GlyfsTer?
ENST00000414678.6:c.952dup ENSP00000412835.2:p.Val318GlyfsTer?
ENST00000452544.1:n.641dup
NM_017519.2:c.2545dup NP_059989.2:p.Val849GlyfsTer?
NM_020732.3:c.2584dup NP_065783.3:p.Val862GlyfsTer?
XM_005267069.3:c.2545dup XP_005267126.2:p.Val849GlyfsTer?
XM_011535984.1:c.1495dup XP_011534286.1:p.Val499GlyfsTer?
XM_011535985.1:c.1315dup XP_011534287.1:p.Val439GlyfsTer?
XM_011535986.1:c.1075dup XP_011534288.1:p.Val359GlyfsTer?
XM_011535987.1:c.694dup XP_011534289.1:p.Val232GlyfsTer?
XM_011535988.1:c.-20+15449dup XP_011534290.1:n.-20+15449dup
NM_001346813.1:c.2545dup NP_001333742.1:p.Val849GlyfsTer?
NM_001363725.1:c.295dup NP_001350654.1:p.Val99GlyfsTer?
XM_011535984.2:c.2626dup XP_011534286.2:p.Val876GlyfsTer?
XM_011535988.3:c.-20+15449dup XP_011534290.1:n.-20+15449dup
XM_017011103.2:c.2626dup XP_016866592.1:p.Val876GlyfsTer?
XM_017011104.1:c.2626dup XP_016866593.1:p.Val876GlyfsTer?
XM_017011105.2:c.2626dup XP_016866594.1:p.Val876GlyfsTer?
XM_017011106.2:c.2626dup XP_016866595.1:p.Val876GlyfsTer?
XM_017011107.2:c.2446dup XP_016866596.1:p.Val816GlyfsTer?
XR_002956289.1:n.2709dup
NM_001363725.2:c.295dup NP_001350654.1:p.Val99GlyfsTer?
NM_001371656.1:c.2833dup NP_001358585.1:p.Val945GlyfsTer?
NM_001374820.1:c.2833dup NP_001361749.1:p.Val945GlyfsTer?
NM_001374828.1:c.2794dup MANE Select NP_001361757.1:p.Val932GlyfsTer?
NM_017519.3:c.2794dup NP_059989.3:p.Val932GlyfsTer?