Canonical Allele Identifier: CA2395734730

Gene: ESS2 TSSK2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19132224_19132225delinsCA , CM000684.2:g.19132224_19132225delinsCA	GRCh38
NC_000022.10:g.19119737_19119738delinsCA , CM000684.1:g.19119737_19119738delinsCA	GRCh37
NC_000022.9:g.17499737_17499738delinsCA	NCBI36
NG_008320.1:g.17453_17454delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252137.11:c.*1971_*1972delinsTG (ESS2) MANE Select	ENSP00000252137.6:n.*1971_*1972delinsTG
ENST00000399635.4:c.825_826delinsCA (TSSK2) MANE Select	ENSP00000382544.2:p.Pro275=
ENST00000252137.10:c.*1971_*1972delinsTG (ESS2)	ENSP00000252137.6:n.*1971_*1972delinsTG
ENST00000399635.3:c.825_826delinsCA (TSSK2)	ENSP00000382544.2:p.Pro275=
NM_022719.2:c.*1971_*1972delinsTG (ESS2)	NP_073210.1:n.*1971_*1972delinsTG
NM_053006.4:c.825_826delinsCA (TSSK2)	NP_443732.3:p.Pro275=
XM_005261282.3:c.*1971_*1972delinsTG (ESS2)	XP_005261339.1:n.*1971_*1972delinsTG
XM_006724329.2:c.*1971_*1972delinsTG (ESS2)	XP_006724392.1:n.*1971_*1972delinsTG
XM_006724330.2:c.*1971_*1972delinsTG (ESS2)	XP_006724393.1:n.*1971_*1972delinsTG
XM_006724331.2:c.*1971_*1972delinsTG (ESS2)	XP_006724394.1:n.*1971_*1972delinsTG
XR_937926.1:n.3360_3361delinsTG (ESS2)
NR_134304.1:n.3516_3517delinsTG (ESS2)
NM_022719.3:c.*1971_*1972delinsTG (ESS2) MANE Select	NP_073210.1:n.*1971_*1972delinsTG
NM_053006.5:c.825_826delinsCA (TSSK2) MANE Select	NP_443732.3:p.Pro275=
NR_134304.2:n.3490_3491delinsTG (ESS2)