Canonical Allele Identifier: CA657685967

Gene: ESS2 TSSK2

Linked Data

• COSMIC: COSN19731032

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19132530_19132531insT , CM000684.2:g.19132530_19132531insT	GRCh38
NC_000022.10:g.19120043_19120044insT , CM000684.1:g.19120043_19120044insT	GRCh37
NC_000022.9:g.17500043_17500044insT	NCBI36
NG_008320.1:g.17147_17148insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252137.11:c.*1665_*1666insA (ESS2) MANE Select	ENSP00000252137.6:n.*1665_*1666insA
ENST00000399635.4:c.*54_*55insT (TSSK2) MANE Select	ENSP00000382544.2:n.*54_*55insT
ENST00000252137.10:c.*1665_*1666insA (ESS2)	ENSP00000252137.6:n.*1665_*1666insA
ENST00000399635.3:c.*54_*55insT (TSSK2)	ENSP00000382544.2:n.*54_*55insT
NM_022719.2:c.*1665_*1666insA (ESS2)	NP_073210.1:n.*1665_*1666insA
NM_053006.4:c.*54_*55insT (TSSK2)	NP_443732.3:n.*54_*55insT
XM_005261282.3:c.*1665_*1666insA (ESS2)	XP_005261339.1:n.*1665_*1666insA
XM_006724329.2:c.*1665_*1666insA (ESS2)	XP_006724392.1:n.*1665_*1666insA
XM_006724330.2:c.*1665_*1666insA (ESS2)	XP_006724393.1:n.*1665_*1666insA
XM_006724331.2:c.*1665_*1666insA (ESS2)	XP_006724394.1:n.*1665_*1666insA
XR_937926.1:n.3054_3055insA (ESS2)
NR_134304.1:n.3210_3211insA (ESS2)
NM_022719.3:c.*1665_*1666insA (ESS2) MANE Select	NP_073210.1:n.*1665_*1666insA
NM_053006.5:c.*54_*55insT (TSSK2) MANE Select	NP_443732.3:n.*54_*55insT
NR_134304.2:n.3184_3185insA (ESS2)