Canonical Allele Identifier: CA2246159925

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121646C= , CM000679.2:g.8121646C=	GRCh38
NC_000017.10:g.8024964C= , CM000679.1:g.8024964C=	GRCh37
NC_000017.9:g.7965689C=	NCBI36
NG_015807.1:g.2271G=
NG_015816.1:g.7447G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.618G= MANE Select	ENSP00000446205.2:p.Pro206=
ENST00000317814.8:c.603G=	ENSP00000314774.4:p.Pro201=
ENST00000541682.6:c.618G=	ENSP00000446205.2:p.Pro206=
NM_001165967.1:c.618G=	NP_001159439.1:p.Pro206=
NM_032580.3:c.603G=	NP_115969.2:p.Pro201=
XM_011524038.1:c.723G=	XP_011522340.1:p.Pro241=
XM_011524039.1:c.714G=	XP_011522341.1:p.Pro238=
XM_011524040.1:c.714G=	XP_011522342.1:p.Pro238=
XM_011524041.1:c.705G=	XP_011522343.1:p.Pro235=
XM_011524042.1:c.576G=	XP_011522344.1:p.Pro192=
XR_934203.1:n.69+1832C=
XM_017025232.1:c.723G=	XP_016880721.1:p.Pro241=
XM_024451007.1:c.723G=	XP_024306775.1:p.Pro241=
NM_001165967.2:c.618G= MANE Select	NP_001159439.1:p.Pro206=
NM_032580.4:c.603G=	NP_115969.2:p.Pro201=