Canonical Allele Identifier: CA2246160890

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122010G= , CM000679.2:g.8122010G=	GRCh38
NC_000017.10:g.8025328G= , CM000679.1:g.8025328G=	GRCh37
NC_000017.9:g.7966053G=	NCBI36
NG_015807.1:g.1907C=
NG_015816.1:g.7083C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.254C= MANE Select	ENSP00000446205.2:p.Ser85=
ENST00000317814.8:c.239C=	ENSP00000314774.4:p.Ser80=
ENST00000541682.6:c.254C=	ENSP00000446205.2:p.Ser85=
ENST00000577735.1:c.230C=	ENSP00000462491.1:p.Ser77=
NM_001165967.1:c.254C=	NP_001159439.1:p.Ser85=
NM_032580.3:c.239C=	NP_115969.2:p.Ser80=
XM_011524038.1:c.359C=	XP_011522340.1:p.Ser120=
XM_011524039.1:c.350C=	XP_011522341.1:p.Ser117=
XM_011524040.1:c.350C=	XP_011522342.1:p.Ser117=
XM_011524041.1:c.341C=	XP_011522343.1:p.Ser114=
XM_011524042.1:c.212C=	XP_011522344.1:p.Ser71=
XR_934203.1:n.69+2196G=
XM_017025232.1:c.359C=	XP_016880721.1:p.Ser120=
XM_024451007.1:c.359C=	XP_024306775.1:p.Ser120=
NM_001165967.2:c.254C= MANE Select	NP_001159439.1:p.Ser85=
NM_032580.4:c.239C=	NP_115969.2:p.Ser80=