Canonical Allele Identifier: CA2246160835

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121981T= , CM000679.2:g.8121981T=	GRCh38
NC_000017.10:g.8025299T= , CM000679.1:g.8025299T=	GRCh37
NC_000017.9:g.7966024T=	NCBI36
NG_015807.1:g.1936A=
NG_015816.1:g.7112A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.283A= MANE Select	ENSP00000446205.2:p.Ser95=
ENST00000317814.8:c.268A=	ENSP00000314774.4:p.Ser90=
ENST00000541682.6:c.283A=	ENSP00000446205.2:p.Ser95=
ENST00000577735.1:c.259A=	ENSP00000462491.1:p.Ser87=
NM_001165967.1:c.283A=	NP_001159439.1:p.Ser95=
NM_032580.3:c.268A=	NP_115969.2:p.Ser90=
XM_011524038.1:c.388A=	XP_011522340.1:p.Ser130=
XM_011524039.1:c.379A=	XP_011522341.1:p.Ser127=
XM_011524040.1:c.379A=	XP_011522342.1:p.Ser127=
XM_011524041.1:c.370A=	XP_011522343.1:p.Ser124=
XM_011524042.1:c.241A=	XP_011522344.1:p.Ser81=
XR_934203.1:n.69+2167T=
XM_017025232.1:c.388A=	XP_016880721.1:p.Ser130=
XM_024451007.1:c.388A=	XP_024306775.1:p.Ser130=
NM_001165967.2:c.283A= MANE Select	NP_001159439.1:p.Ser95=
NM_032580.4:c.268A=	NP_115969.2:p.Ser90=