Canonical Allele Identifier: CA1675486513

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157083448_157083449delinsTG , CM000668.2:g.157083448_157083449delinsTG	GRCh38
NC_000006.11:g.157404582_157404583delinsTG , CM000668.1:g.157404582_157404583delinsTG	GRCh37
NC_000006.10:g.157446274_157446275delinsTG	NCBI36
NG_032093.1:g.310519_310520delinsTG
NG_032093.2:g.310519_310520delinsTG
NG_066624.1:g.312423_312424delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2248-1214_2248-1213delinsTG	ENSP00000055163.8:n.2248-1214_2248-1213delinsTG
ENST00000414678.8:c.2248-1214_2248-1213delinsTG	ENSP00000412835.3:n.2248-1214_2248-1213delinsTG
ENST00000637015.2:c.2248-1214_2248-1213delinsTG	ENSP00000489729.2:n.2248-1214_2248-1213delinsTG
ENST00000319584.11:c.262-1214_262-1213delinsTG	ENSP00000313006.7:n.262-1214_262-1213delinsTG
ENST00000346085.10:c.2287-1214_2287-1213delinsTG	ENSP00000344546.5:n.2287-1214_2287-1213delinsTG
ENST00000350026.10:c.1999-1214_1999-1213delinsTG	ENSP00000055163.7:n.1999-1214_1999-1213delinsTG
ENST00000414678.7:c.496-1214_496-1213delinsTG	ENSP00000412835.2:n.496-1214_496-1213delinsTG
ENST00000452544.2:n.149-1214_149-1213delinsTG
ENST00000635849.1:c.-252-1214_-252-1213delinsTG	ENSP00000490948.1:n.-252-1214_-252-1213delinsTG
ENST00000636930.2:c.2248-1214_2248-1213delinsTG MANE Select	ENSP00000490491.2:n.2248-1214_2248-1213delinsTG
ENST00000637003.1:c.-252-1214_-252-1213delinsTG	ENSP00000489666.1:n.-252-1214_-252-1213delinsTG
ENST00000637904.1:c.-252-1214_-252-1213delinsTG	ENSP00000490550.1:n.-252-1214_-252-1213delinsTG
ENST00000647938.1:c.2038-1214_2038-1213delinsTG	ENSP00000498155.1:n.2038-1214_2038-1213delinsTG
ENST00000674190.1:n.997-1214_997-1213delinsTG
ENST00000319584.10:c.265-1214_265-1213delinsTG	ENSP00000313006.6:n.265-1214_265-1213delinsTG
ENST00000346085.9:c.2038-1214_2038-1213delinsTG	ENSP00000344546.4:n.2038-1214_2038-1213delinsTG
ENST00000350026.9:c.1999-1214_1999-1213delinsTG	ENSP00000055163.7:n.1999-1214_1999-1213delinsTG
ENST00000414678.6:c.496-1214_496-1213delinsTG	ENSP00000412835.2:n.496-1214_496-1213delinsTG
ENST00000452544.1:n.107-1214_107-1213delinsTG
NM_017519.2:c.1999-1214_1999-1213delinsTG	NP_059989.2:n.1999-1214_1999-1213delinsTG
NM_020732.3:c.2038-1214_2038-1213delinsTG	NP_065783.3:n.2038-1214_2038-1213delinsTG
XM_005267069.3:c.1999-1214_1999-1213delinsTG	XP_005267126.2:n.1999-1214_1999-1213delinsTG
XM_011535984.1:c.949-1214_949-1213delinsTG	XP_011534286.1:n.949-1214_949-1213delinsTG
XM_011535985.1:c.949-1214_949-1213delinsTG	XP_011534287.1:n.949-1214_949-1213delinsTG
XM_011535986.1:c.529-1214_529-1213delinsTG	XP_011534288.1:n.529-1214_529-1213delinsTG
XM_011535987.1:c.148-1214_148-1213delinsTG	XP_011534289.1:n.148-1214_148-1213delinsTG
NM_001346813.1:c.1999-1214_1999-1213delinsTG	NP_001333742.1:n.1999-1214_1999-1213delinsTG
NM_001363725.1:c.-252-1214_-252-1213delinsTG	NP_001350654.1:n.-252-1214_-252-1213delinsTG
XM_011535984.2:c.2080-1214_2080-1213delinsTG	XP_011534286.2:n.2080-1214_2080-1213delinsTG
XM_017011103.2:c.2080-1214_2080-1213delinsTG	XP_016866592.1:n.2080-1214_2080-1213delinsTG
XM_017011104.1:c.2080-1214_2080-1213delinsTG	XP_016866593.1:n.2080-1214_2080-1213delinsTG
XM_017011105.2:c.2080-1214_2080-1213delinsTG	XP_016866594.1:n.2080-1214_2080-1213delinsTG
XM_017011106.2:c.2080-1214_2080-1213delinsTG	XP_016866595.1:n.2080-1214_2080-1213delinsTG
XM_017011107.2:c.2080-1214_2080-1213delinsTG	XP_016866596.1:n.2080-1214_2080-1213delinsTG
XR_002956289.1:n.2163-1214_2163-1213delinsTG
NM_001363725.2:c.-252-1214_-252-1213delinsTG	NP_001350654.1:n.-252-1214_-252-1213delinsTG
NM_001371656.1:c.2287-1214_2287-1213delinsTG	NP_001358585.1:n.2287-1214_2287-1213delinsTG
NM_001374820.1:c.2287-1214_2287-1213delinsTG	NP_001361749.1:n.2287-1214_2287-1213delinsTG
NM_001374828.1:c.2248-1214_2248-1213delinsTG MANE Select	NP_001361757.1:n.2248-1214_2248-1213delinsTG
NM_017519.3:c.2248-1214_2248-1213delinsTG	NP_059989.3:n.2248-1214_2248-1213delinsTG