Canonical Allele Identifier: CA2246159810

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121598C= , CM000679.2:g.8121598C=	GRCh38
NC_000017.10:g.8024916C= , CM000679.1:g.8024916C=	GRCh37
NC_000017.9:g.7965641C=	NCBI36
NG_015807.1:g.2319G=
NG_015816.1:g.7495G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.666G= MANE Select	ENSP00000446205.2:p.Pro222=
ENST00000317814.8:c.651G=	ENSP00000314774.4:p.Pro217=
ENST00000541682.6:c.666G=	ENSP00000446205.2:p.Pro222=
NM_001165967.1:c.666G=	NP_001159439.1:p.Pro222=
NM_032580.3:c.651G=	NP_115969.2:p.Pro217=
XM_011524038.1:c.771G=	XP_011522340.1:p.Pro257=
XM_011524039.1:c.762G=	XP_011522341.1:p.Pro254=
XM_011524040.1:c.762G=	XP_011522342.1:p.Pro254=
XM_011524041.1:c.753G=	XP_011522343.1:p.Pro251=
XM_011524042.1:c.624G=	XP_011522344.1:p.Pro208=
XR_934203.1:n.69+1784C=
XM_017025232.1:c.771G=	XP_016880721.1:p.Pro257=
XM_024451007.1:c.771G=	XP_024306775.1:p.Pro257=
NM_001165967.2:c.666G= MANE Select	NP_001159439.1:p.Pro222=
NM_032580.4:c.651G=	NP_115969.2:p.Pro217=