Canonical Allele Identifier: CA2246159855

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121623G= , CM000679.2:g.8121623G=	GRCh38
NC_000017.10:g.8024941G= , CM000679.1:g.8024941G=	GRCh37
NC_000017.9:g.7965666G=	NCBI36
NG_015807.1:g.2294C=
NG_015816.1:g.7470C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.641C= MANE Select	ENSP00000446205.2:p.Ala214=
ENST00000317814.8:c.626C=	ENSP00000314774.4:p.Ala209=
ENST00000541682.6:c.641C=	ENSP00000446205.2:p.Ala214=
NM_001165967.1:c.641C=	NP_001159439.1:p.Ala214=
NM_032580.3:c.626C=	NP_115969.2:p.Ala209=
XM_011524038.1:c.746C=	XP_011522340.1:p.Ala249=
XM_011524039.1:c.737C=	XP_011522341.1:p.Ala246=
XM_011524040.1:c.737C=	XP_011522342.1:p.Ala246=
XM_011524041.1:c.728C=	XP_011522343.1:p.Ala243=
XM_011524042.1:c.599C=	XP_011522344.1:p.Ala200=
XR_934203.1:n.69+1809G=
XM_017025232.1:c.746C=	XP_016880721.1:p.Ala249=
XM_024451007.1:c.746C=	XP_024306775.1:p.Ala249=
NM_001165967.2:c.641C= MANE Select	NP_001159439.1:p.Ala214=
NM_032580.4:c.626C=	NP_115969.2:p.Ala209=