Canonical Allele Identifier: CA2395734694

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19132147T= , CM000684.2:g.19132147T= GRCh38
NC_000022.10:g.19119660T= , CM000684.1:g.19119660T= GRCh37
NC_000022.9:g.17499660T= NCBI36
NG_008320.1:g.17531A=

Transcript Alleles

HGVS Amino-acid change
ENST00000252137.11:c.*2049A= (ESS2) MANE Select ENSP00000252137.6:n.*2049A=
ENST00000399635.4:c.748T= (TSSK2) MANE Select ENSP00000382544.2:p.Tyr250=
ENST00000252137.10:c.*2049A= (ESS2) ENSP00000252137.6:n.*2049A=
ENST00000399635.3:c.748T= (TSSK2) ENSP00000382544.2:p.Tyr250=
NM_022719.2:c.*2049A= (ESS2) NP_073210.1:n.*2049A=
NM_053006.4:c.748T= (TSSK2) NP_443732.3:p.Tyr250=
XM_005261282.3:c.*2049A= (ESS2) XP_005261339.1:n.*2049A=
XM_006724329.2:c.*2049A= (ESS2) XP_006724392.1:n.*2049A=
XM_006724330.2:c.*2049A= (ESS2) XP_006724393.1:n.*2049A=
XM_006724331.2:c.*2049A= (ESS2) XP_006724394.1:n.*2049A=
XR_937926.1:n.3438A= (ESS2)
NR_134304.1:n.3594A= (ESS2)
NM_022719.3:c.*2049A= (ESS2) MANE Select NP_073210.1:n.*2049A=
NM_053006.5:c.748T= (TSSK2) MANE Select NP_443732.3:p.Tyr250=
NR_134304.2:n.3568A= (ESS2)