Canonical Allele Identifier: CA2246159962

Gene: HES7

Linked Data

• dbSNP Id: rs1981329847

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121656_8121661dup , CM000679.2:g.8121656_8121661dup	GRCh38
NC_000017.10:g.8024974_8024979dup , CM000679.1:g.8024974_8024979dup	GRCh37
NC_000017.9:g.7965699_7965704dup	NCBI36
NG_015807.1:g.2258_2263dup
NG_015816.1:g.7434_7439dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.605_610dup MANE Select	ENSP00000446205.2:p.Pro203_Pro204insLeuPro
ENST00000317814.8:c.590_595dup	ENSP00000314774.4:p.Pro198_Pro199insLeuPro
ENST00000541682.6:c.605_610dup	ENSP00000446205.2:p.Pro203_Pro204insLeuPro
NM_001165967.1:c.605_610dup	NP_001159439.1:p.Pro203_Pro204insLeuPro
NM_032580.3:c.590_595dup	NP_115969.2:p.Pro198_Pro199insLeuPro
XM_011524038.1:c.710_715dup	XP_011522340.1:p.Pro238_Pro239insLeuPro
XM_011524039.1:c.701_706dup	XP_011522341.1:p.Pro235_Pro236insLeuPro
XM_011524040.1:c.701_706dup	XP_011522342.1:p.Pro235_Pro236insLeuPro
XM_011524041.1:c.692_697dup	XP_011522343.1:p.Pro232_Pro233insLeuPro
XM_011524042.1:c.563_568dup	XP_011522344.1:p.Pro189_Pro190insLeuPro
XR_934203.1:n.69+1842_69+1847dup
XM_017025232.1:c.710_715dup	XP_016880721.1:p.Pro238_Pro239insLeuPro
XM_024451007.1:c.710_715dup	XP_024306775.1:p.Pro238_Pro239insLeuPro
NM_001165967.2:c.605_610dup MANE Select	NP_001159439.1:p.Pro203_Pro204insLeuPro
NM_032580.4:c.590_595dup	NP_115969.2:p.Pro198_Pro199insLeuPro