Canonical Allele Identifier: CA2655248461

Gene: ESS2 TSSK2

Linked Data

• gnomAD v4: 22-19132539-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19132539_19132540insG , CM000684.2:g.19132539_19132540insG	GRCh38
NC_000022.10:g.19120052_19120053insG , CM000684.1:g.19120052_19120053insG	GRCh37
NC_000022.9:g.17500052_17500053insG	NCBI36
NG_008320.1:g.17138_17139insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252137.11:c.*1656_*1657insC (ESS2) MANE Select	ENSP00000252137.6:n.*1656_*1657insC
ENST00000399635.4:c.*63_*64insG (TSSK2) MANE Select	ENSP00000382544.2:n.*63_*64insG
ENST00000252137.10:c.*1656_*1657insC (ESS2)	ENSP00000252137.6:n.*1656_*1657insC
ENST00000399635.3:c.*63_*64insG (TSSK2)	ENSP00000382544.2:n.*63_*64insG
NM_022719.2:c.*1656_*1657insC (ESS2)	NP_073210.1:n.*1656_*1657insC
NM_053006.4:c.*63_*64insG (TSSK2)	NP_443732.3:n.*63_*64insG
XM_005261282.3:c.*1656_*1657insC (ESS2)	XP_005261339.1:n.*1656_*1657insC
XM_006724329.2:c.*1656_*1657insC (ESS2)	XP_006724392.1:n.*1656_*1657insC
XM_006724330.2:c.*1656_*1657insC (ESS2)	XP_006724393.1:n.*1656_*1657insC
XM_006724331.2:c.*1656_*1657insC (ESS2)	XP_006724394.1:n.*1656_*1657insC
XR_937926.1:n.3045_3046insC (ESS2)
NR_134304.1:n.3201_3202insC (ESS2)
NM_022719.3:c.*1656_*1657insC (ESS2) MANE Select	NP_073210.1:n.*1656_*1657insC
NM_053006.5:c.*63_*64insG (TSSK2) MANE Select	NP_443732.3:n.*63_*64insG
NR_134304.2:n.3175_3176insC (ESS2)