Canonical Allele Identifier: CA638335885

Gene: ESS2 TSSK2

Linked Data

• dbSNP Id: rs1467205857
• gnomAD v2: 22-19119996-A-G
• gnomAD v4: 22-19132483-A-G
• MyVariant Identifiers: chr22:g.19119996A>G (hg19) ; chr22:g.19132483A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19132483A>G , CM000684.2:g.19132483A>G	GRCh38
NC_000022.10:g.19119996A>G , CM000684.1:g.19119996A>G	GRCh37
NC_000022.9:g.17499996A>G	NCBI36
NG_008320.1:g.17195T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252137.11:c.*1713T>C (ESS2) MANE Select	ENSP00000252137.6:n.*1713T>C
ENST00000399635.4:c.*7A>G (TSSK2) MANE Select	ENSP00000382544.2:n.*7A>G
ENST00000252137.10:c.*1713T>C (ESS2)	ENSP00000252137.6:n.*1713T>C
ENST00000399635.3:c.*7A>G (TSSK2)	ENSP00000382544.2:n.*7A>G
NM_022719.2:c.*1713T>C (ESS2)	NP_073210.1:n.*1713T>C
NM_053006.4:c.*7A>G (TSSK2)	NP_443732.3:n.*7A>G
XM_005261282.3:c.*1713T>C (ESS2)	XP_005261339.1:n.*1713T>C
XM_006724329.2:c.*1713T>C (ESS2)	XP_006724392.1:n.*1713T>C
XM_006724330.2:c.*1713T>C (ESS2)	XP_006724393.1:n.*1713T>C
XM_006724331.2:c.*1713T>C (ESS2)	XP_006724394.1:n.*1713T>C
XR_937926.1:n.3102T>C (ESS2)
NR_134304.1:n.3258T>C (ESS2)
NM_022719.3:c.*1713T>C (ESS2) MANE Select	NP_073210.1:n.*1713T>C
NM_053006.5:c.*7A>G (TSSK2) MANE Select	NP_443732.3:n.*7A>G
NR_134304.2:n.3232T>C (ESS2)