Canonical Allele Identifier: CA397988783

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8025287A>T (hg19) ; chr17:g.8121969A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121969A>T , CM000679.2:g.8121969A>T	GRCh38
NC_000017.10:g.8025287A>T , CM000679.1:g.8025287A>T	GRCh37
NC_000017.9:g.7966012A>T	NCBI36
NG_015807.1:g.1948T>A
NG_015816.1:g.7124T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.295T>A MANE Select	ENSP00000446205.2:p.Ser99Thr
ENST00000317814.8:c.280T>A	ENSP00000314774.4:p.Ser94Thr
ENST00000541682.6:c.295T>A	ENSP00000446205.2:p.Ser99Thr
ENST00000577735.1:c.271T>A	ENSP00000462491.1:p.Ser91Thr
NM_001165967.1:c.295T>A	NP_001159439.1:p.Ser99Thr
NM_032580.3:c.280T>A	NP_115969.2:p.Ser94Thr
XM_011524038.1:c.400T>A	XP_011522340.1:p.Ser134Thr
XM_011524039.1:c.391T>A	XP_011522341.1:p.Ser131Thr
XM_011524040.1:c.391T>A	XP_011522342.1:p.Ser131Thr
XM_011524041.1:c.382T>A	XP_011522343.1:p.Ser128Thr
XM_011524042.1:c.253T>A	XP_011522344.1:p.Ser85Thr
XR_934203.1:n.69+2155A>T
XM_017025232.1:c.400T>A	XP_016880721.1:p.Ser134Thr
XM_024451007.1:c.400T>A	XP_024306775.1:p.Ser134Thr
NM_001165967.2:c.295T>A MANE Select	NP_001159439.1:p.Ser99Thr
NM_032580.4:c.280T>A	NP_115969.2:p.Ser94Thr