Canonical Allele Identifier: CA2395734872

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19132502_19132503delinsGT , CM000684.2:g.19132502_19132503delinsGT GRCh38
NC_000022.10:g.19120015_19120016delinsGT , CM000684.1:g.19120015_19120016delinsGT GRCh37
NC_000022.9:g.17500015_17500016delinsGT NCBI36
NG_008320.1:g.17175_17176delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000252137.11:c.*1693_*1694delinsAC (ESS2) MANE Select ENSP00000252137.6:n.*1693_*1694delinsAC
ENST00000399635.4:c.*26_*27delinsGT (TSSK2) MANE Select ENSP00000382544.2:n.*26_*27delinsGT
ENST00000252137.10:c.*1693_*1694delinsAC (ESS2) ENSP00000252137.6:n.*1693_*1694delinsAC
ENST00000399635.3:c.*26_*27delinsGT (TSSK2) ENSP00000382544.2:n.*26_*27delinsGT
NM_022719.2:c.*1693_*1694delinsAC (ESS2) NP_073210.1:n.*1693_*1694delinsAC
NM_053006.4:c.*26_*27delinsGT (TSSK2) NP_443732.3:n.*26_*27delinsGT
XM_005261282.3:c.*1693_*1694delinsAC (ESS2) XP_005261339.1:n.*1693_*1694delinsAC
XM_006724329.2:c.*1693_*1694delinsAC (ESS2) XP_006724392.1:n.*1693_*1694delinsAC
XM_006724330.2:c.*1693_*1694delinsAC (ESS2) XP_006724393.1:n.*1693_*1694delinsAC
XM_006724331.2:c.*1693_*1694delinsAC (ESS2) XP_006724394.1:n.*1693_*1694delinsAC
XR_937926.1:n.3082_3083delinsAC (ESS2)
NR_134304.1:n.3238_3239delinsAC (ESS2)
NM_022719.3:c.*1693_*1694delinsAC (ESS2) MANE Select NP_073210.1:n.*1693_*1694delinsAC
NM_053006.5:c.*26_*27delinsGT (TSSK2) MANE Select NP_443732.3:n.*26_*27delinsGT
NR_134304.2:n.3212_3213delinsAC (ESS2)