Canonical Allele Identifier: CA366005872

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149400597G>T , CM000668.2:g.149400597G>T GRCh38
NC_000006.11:g.149721733G>T , CM000668.1:g.149721733G>T GRCh37
NC_000006.10:g.149763426G>T NCBI36
NG_012301.1:g.5239G>T
NG_021386.1:g.87298G>T
NG_021386.2:g.187674G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326669.6:c.206G>T (SUMO4) MANE Select ENSP00000318635.4:p.Gly69Val
ENST00000636456.1:c.1087+1413G>T (TAB2) ENSP00000490379.1:n.1087+1413G>T
ENST00000637181.2:c.1939+1413G>T (TAB2) MANE Select ENSP00000490618.1:n.1939+1413G>T
ENST00000326669.5:c.206G>T (SUMO4) ENSP00000318635.4:p.Gly69Val
ENST00000367456.5:c.1939+1413G>T (TAB2) ENSP00000356426.1:n.1939+1413G>T
ENST00000470466.5:c.*538+1413G>T (TAB2) ENSP00000432709.1:n.*538+1413G>T
ENST00000484505.1:n.452+1413G>T (TAB2)
ENST00000538427.5:c.1939+1413G>T (TAB2) ENSP00000445752.1:n.1939+1413G>T
NM_001002255.1:c.206G>T (SUMO4) NP_001002255.1:p.Gly69Val
NM_001292034.2:c.1939+1413G>T (TAB2) NP_001278963.1:n.1939+1413G>T
NM_001292035.2:c.1843+1413G>T (TAB2) NP_001278964.1:n.1843+1413G>T
NM_015093.5:c.1939+1413G>T (TAB2) NP_055908.1:n.1939+1413G>T
XM_006715403.2:c.1939+1413G>T (TAB2) XP_006715466.1:n.1939+1413G>T
XM_011535633.1:c.1939+1413G>T (TAB2) XP_011533935.1:n.1939+1413G>T
XM_011535634.1:c.1939+1413G>T (TAB2) XP_011533936.1:n.1939+1413G>T
XM_011535633.2:c.1939+1413G>T (TAB2) XP_011533935.1:n.1939+1413G>T
XM_017010591.1:c.1939+1413G>T (TAB2) XP_016866080.1:n.1939+1413G>T
XM_017010592.2:c.1939+1413G>T (TAB2) XP_016866081.1:n.1939+1413G>T
NM_001292034.3:c.1939+1413G>T (TAB2) MANE Select NP_001278963.1:n.1939+1413G>T
NM_001002255.2:c.206G>T (SUMO4) MANE Select NP_001002255.1:p.Gly69Val
NM_001292035.3:c.1843+1413G>T (TAB2) NP_001278964.1:n.1843+1413G>T
NM_001369506.1:c.1939+1413G>T (TAB2) NP_001356435.1:n.1939+1413G>T
NM_015093.6:c.1939+1413G>T (TAB2) NP_055908.1:n.1939+1413G>T