Canonical Allele Identifier: CA2246160807

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121971A= , CM000679.2:g.8121971A=	GRCh38
NC_000017.10:g.8025289A= , CM000679.1:g.8025289A=	GRCh37
NC_000017.9:g.7966014A=	NCBI36
NG_015807.1:g.1946T=
NG_015816.1:g.7122T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.293T= MANE Select	ENSP00000446205.2:p.Leu98=
ENST00000317814.8:c.278T=	ENSP00000314774.4:p.Leu93=
ENST00000541682.6:c.293T=	ENSP00000446205.2:p.Leu98=
ENST00000577735.1:c.269T=	ENSP00000462491.1:p.Leu90=
NM_001165967.1:c.293T=	NP_001159439.1:p.Leu98=
NM_032580.3:c.278T=	NP_115969.2:p.Leu93=
XM_011524038.1:c.398T=	XP_011522340.1:p.Leu133=
XM_011524039.1:c.389T=	XP_011522341.1:p.Leu130=
XM_011524040.1:c.389T=	XP_011522342.1:p.Leu130=
XM_011524041.1:c.380T=	XP_011522343.1:p.Leu127=
XM_011524042.1:c.251T=	XP_011522344.1:p.Leu84=
XR_934203.1:n.69+2157A=
XM_017025232.1:c.398T=	XP_016880721.1:p.Leu133=
XM_024451007.1:c.398T=	XP_024306775.1:p.Leu133=
NM_001165967.2:c.293T= MANE Select	NP_001159439.1:p.Leu98=
NM_032580.4:c.278T=	NP_115969.2:p.Leu93=