Canonical Allele Identifier: CA2246162739

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8123096G= , CM000679.2:g.8123096G=	GRCh38
NC_000017.10:g.8026414G= , CM000679.1:g.8026414G=	GRCh37
NC_000017.9:g.7967139G=	NCBI36
NG_015807.1:g.821C=
NG_015816.1:g.5997C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001165967.2:c.73C= MANE Select	NP_001159439.1:p.Arg25=
ENST00000541682.7:c.73C= MANE Select	ENSP00000446205.2:p.Arg25=
NM_001165967.1:c.73C=	NP_001159439.1:p.Arg25=
NM_032580.3:c.73C=	NP_115969.2:p.Arg25=
NM_032580.4:c.73C=	NP_115969.2:p.Arg25=
ENST00000317814.8:c.73C=	ENSP00000314774.4:p.Arg25=
ENST00000541682.6:c.73C=	ENSP00000446205.2:p.Arg25=
ENST00000577735.1:c.49C=	ENSP00000462491.1:p.Arg17=
XM_011524038.1:c.178C=	XP_011522340.1:p.Arg60=
XM_011524039.1:c.169C=	XP_011522341.1:p.Arg57=
XM_011524040.1:c.169C=	XP_011522342.1:p.Arg57=
XM_011524041.1:c.160C=	XP_011522343.1:p.Arg54=
XM_011524042.1:c.31C=	XP_011522344.1:p.Arg11=
XM_017025232.1:c.178C=	XP_016880721.1:p.Arg60=
XM_024451007.1:c.178C=	XP_024306775.1:p.Arg60=
XR_934203.1:n.69+3282G=