Canonical Allele Identifier: CA2987128655

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19131962_19131963insTAT , CM000684.2:g.19131962_19131963insTAT GRCh38
NC_000022.10:g.19119475_19119476insTAT , CM000684.1:g.19119475_19119476insTAT GRCh37
NC_000022.9:g.17499475_17499476insTAT NCBI36
NG_008320.1:g.17715_17716insATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000252137.11:c.*2233_*2234insATA (ESS2) MANE Select ENSP00000252137.6:n.*2233_*2234insATA
ENST00000399635.4:c.563_564insTAT (TSSK2) MANE Select ENSP00000382544.2:p.Gln188delinsHisMet
ENST00000252137.10:c.*2233_*2234insATA (ESS2) ENSP00000252137.6:n.*2233_*2234insATA
ENST00000399635.3:c.563_564insTAT (TSSK2) ENSP00000382544.2:p.Gln188delinsHisMet
NM_022719.2:c.*2233_*2234insATA (ESS2) NP_073210.1:n.*2233_*2234insATA
NM_053006.4:c.563_564insTAT (TSSK2) NP_443732.3:p.Gln188delinsHisMet
XM_005261282.3:c.*2233_*2234insATA (ESS2) XP_005261339.1:n.*2233_*2234insATA
XM_006724329.2:c.*2233_*2234insATA (ESS2) XP_006724392.1:n.*2233_*2234insATA
XM_006724330.2:c.*2233_*2234insATA (ESS2) XP_006724393.1:n.*2233_*2234insATA
XM_006724331.2:c.*2233_*2234insATA (ESS2) XP_006724394.1:n.*2233_*2234insATA
XR_937926.1:n.3622_3623insATA (ESS2)
NR_134304.1:n.3778_3779insATA (ESS2)
NM_022719.3:c.*2233_*2234insATA (ESS2) MANE Select NP_073210.1:n.*2233_*2234insATA
NM_053006.5:c.563_564insTAT (TSSK2) MANE Select NP_443732.3:p.Gln188delinsHisMet
NR_134304.2:n.3752_3753insATA (ESS2)