Canonical Allele Identifier: CA2551064236

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121541dup , CM000679.2:g.8121541dup	GRCh38
NC_000017.10:g.8024859dup , CM000679.1:g.8024859dup	GRCh37
NC_000017.9:g.7965584dup	NCBI36
NG_015807.1:g.2379dup
NG_015816.1:g.7555dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*33dup MANE Select	ENSP00000446205.2:n.*33dup
ENST00000541682.6:c.726dup	ENSP00000446205.2:n.726dup
NM_001165967.1:c.*33dup	NP_001159439.1:n.*33dup
NM_032580.3:c.*33dup	NP_115969.2:n.*33dup
XM_011524038.1:c.*33dup	XP_011522340.1:n.*33dup
XM_011524039.1:c.*33dup	XP_011522341.1:n.*33dup
XM_011524040.1:c.*33dup	XP_011522342.1:n.*33dup
XM_011524041.1:c.*33dup	XP_011522343.1:n.*33dup
XM_011524042.1:c.*33dup	XP_011522344.1:n.*33dup
XR_934203.1:n.69+1727dup
XM_017025232.1:c.*33dup	XP_016880721.1:n.*33dup
XM_024451007.1:c.*33dup	XP_024306775.1:n.*33dup
NM_001165967.2:c.*33dup MANE Select	NP_001159439.1:n.*33dup
NM_032580.4:c.*33dup	NP_115969.2:n.*33dup