Canonical Allele Identifier: CA2395734811

Gene: ESS2 TSSK2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19132383G= , CM000684.2:g.19132383G=	GRCh38
NC_000022.10:g.19119896G= , CM000684.1:g.19119896G=	GRCh37
NC_000022.9:g.17499896G=	NCBI36
NG_008320.1:g.17295C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252137.11:c.*1813C= (ESS2) MANE Select	ENSP00000252137.6:n.*1813C=
ENST00000399635.4:c.984G= (TSSK2) MANE Select	ENSP00000382544.2:p.Glu328=
ENST00000252137.10:c.*1813C= (ESS2)	ENSP00000252137.6:n.*1813C=
ENST00000399635.3:c.984G= (TSSK2)	ENSP00000382544.2:p.Glu328=
NM_022719.2:c.*1813C= (ESS2)	NP_073210.1:n.*1813C=
NM_053006.4:c.984G= (TSSK2)	NP_443732.3:p.Glu328=
XM_005261282.3:c.*1813C= (ESS2)	XP_005261339.1:n.*1813C=
XM_006724329.2:c.*1813C= (ESS2)	XP_006724392.1:n.*1813C=
XM_006724330.2:c.*1813C= (ESS2)	XP_006724393.1:n.*1813C=
XM_006724331.2:c.*1813C= (ESS2)	XP_006724394.1:n.*1813C=
XR_937926.1:n.3202C= (ESS2)
NR_134304.1:n.3358C= (ESS2)
NM_022719.3:c.*1813C= (ESS2) MANE Select	NP_073210.1:n.*1813C=
NM_053006.5:c.984G= (TSSK2) MANE Select	NP_443732.3:p.Glu328=
NR_134304.2:n.3332C= (ESS2)