Canonical Allele Identifier: CA2246160895

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122013C= , CM000679.2:g.8122013C=	GRCh38
NC_000017.10:g.8025331C= , CM000679.1:g.8025331C=	GRCh37
NC_000017.9:g.7966056C=	NCBI36
NG_015807.1:g.1904G=
NG_015816.1:g.7080G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.251G= MANE Select	ENSP00000446205.2:p.Arg84=
ENST00000317814.8:c.236G=	ENSP00000314774.4:p.Arg79=
ENST00000541682.6:c.251G=	ENSP00000446205.2:p.Arg84=
ENST00000577735.1:c.227G=	ENSP00000462491.1:p.Arg76=
NM_001165967.1:c.251G=	NP_001159439.1:p.Arg84=
NM_032580.3:c.236G=	NP_115969.2:p.Arg79=
XM_011524038.1:c.356G=	XP_011522340.1:p.Arg119=
XM_011524039.1:c.347G=	XP_011522341.1:p.Arg116=
XM_011524040.1:c.347G=	XP_011522342.1:p.Arg116=
XM_011524041.1:c.338G=	XP_011522343.1:p.Arg113=
XM_011524042.1:c.209G=	XP_011522344.1:p.Arg70=
XR_934203.1:n.69+2199C=
XM_017025232.1:c.356G=	XP_016880721.1:p.Arg119=
XM_024451007.1:c.356G=	XP_024306775.1:p.Arg119=
NM_001165967.2:c.251G= MANE Select	NP_001159439.1:p.Arg84=
NM_032580.4:c.236G=	NP_115969.2:p.Arg79=