Canonical Allele Identifier: CA513187311

Gene: ESS2 TSSK2

Linked Data

• MyVariant Identifiers: chr22:g.19119921C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19132408C>T , CM000684.2:g.19132408C>T	GRCh38
NC_000022.10:g.19119921C>T , CM000684.1:g.19119921C>T	GRCh37
NC_000022.9:g.17499921C>T	NCBI36
NG_008320.1:g.17270G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252137.11:c.*1788G>A (ESS2) MANE Select	ENSP00000252137.6:n.*1788G>A
ENST00000399635.4:c.1009C>T (TSSK2) MANE Select	ENSP00000382544.2:p.Leu337=
ENST00000252137.10:c.*1788G>A (ESS2)	ENSP00000252137.6:n.*1788G>A
ENST00000399635.3:c.1009C>T (TSSK2)	ENSP00000382544.2:p.Leu337=
NM_022719.2:c.*1788G>A (ESS2)	NP_073210.1:n.*1788G>A
NM_053006.4:c.1009C>T (TSSK2)	NP_443732.3:p.Leu337=
XM_005261282.3:c.*1788G>A (ESS2)	XP_005261339.1:n.*1788G>A
XM_006724329.2:c.*1788G>A (ESS2)	XP_006724392.1:n.*1788G>A
XM_006724330.2:c.*1788G>A (ESS2)	XP_006724393.1:n.*1788G>A
XM_006724331.2:c.*1788G>A (ESS2)	XP_006724394.1:n.*1788G>A
XR_937926.1:n.3177G>A (ESS2)
NR_134304.1:n.3333G>A (ESS2)
NM_022719.3:c.*1788G>A (ESS2) MANE Select	NP_073210.1:n.*1788G>A
NM_053006.5:c.1009C>T (TSSK2) MANE Select	NP_443732.3:p.Leu337=
NR_134304.2:n.3307G>A (ESS2)