Canonical Allele Identifier: CA2246159832

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121610C= , CM000679.2:g.8121610C=	GRCh38
NC_000017.10:g.8024928C= , CM000679.1:g.8024928C=	GRCh37
NC_000017.9:g.7965653C=	NCBI36
NG_015807.1:g.2307G=
NG_015816.1:g.7483G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.654G= MANE Select	ENSP00000446205.2:p.Pro218=
ENST00000317814.8:c.639G=	ENSP00000314774.4:p.Pro213=
ENST00000541682.6:c.654G=	ENSP00000446205.2:p.Pro218=
NM_001165967.1:c.654G=	NP_001159439.1:p.Pro218=
NM_032580.3:c.639G=	NP_115969.2:p.Pro213=
XM_011524038.1:c.759G=	XP_011522340.1:p.Pro253=
XM_011524039.1:c.750G=	XP_011522341.1:p.Pro250=
XM_011524040.1:c.750G=	XP_011522342.1:p.Pro250=
XM_011524041.1:c.741G=	XP_011522343.1:p.Pro247=
XM_011524042.1:c.612G=	XP_011522344.1:p.Pro204=
XR_934203.1:n.69+1796C=
XM_017025232.1:c.759G=	XP_016880721.1:p.Pro253=
XM_024451007.1:c.759G=	XP_024306775.1:p.Pro253=
NM_001165967.2:c.654G= MANE Select	NP_001159439.1:p.Pro218=
NM_032580.4:c.639G=	NP_115969.2:p.Pro213=