Canonical Allele Identifier: CA2246160701

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121935G= , CM000679.2:g.8121935G=	GRCh38
NC_000017.10:g.8025253G= , CM000679.1:g.8025253G=	GRCh37
NC_000017.9:g.7965978G=	NCBI36
NG_015807.1:g.1982C=
NG_015816.1:g.7158C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.329C= MANE Select	ENSP00000446205.2:p.Ala110=
ENST00000317814.8:c.314C=	ENSP00000314774.4:p.Ala105=
ENST00000541682.6:c.329C=	ENSP00000446205.2:p.Ala110=
ENST00000577735.1:c.305C=	ENSP00000462491.1:p.Ala102=
NM_001165967.1:c.329C=	NP_001159439.1:p.Ala110=
NM_032580.3:c.314C=	NP_115969.2:p.Ala105=
XM_011524038.1:c.434C=	XP_011522340.1:p.Ala145=
XM_011524039.1:c.425C=	XP_011522341.1:p.Ala142=
XM_011524040.1:c.425C=	XP_011522342.1:p.Ala142=
XM_011524041.1:c.416C=	XP_011522343.1:p.Ala139=
XM_011524042.1:c.287C=	XP_011522344.1:p.Ala96=
XR_934203.1:n.69+2121G=
XM_017025232.1:c.434C=	XP_016880721.1:p.Ala145=
XM_024451007.1:c.434C=	XP_024306775.1:p.Ala145=
NM_001165967.2:c.329C= MANE Select	NP_001159439.1:p.Ala110=
NM_032580.4:c.314C=	NP_115969.2:p.Ala105=