Canonical Allele Identifier: CA2635936679

Gene: HES7

Linked Data

• gnomAD v4: 17-8121601-C-CGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121604_8121606dup , CM000679.2:g.8121604_8121606dup	GRCh38
NC_000017.10:g.8024922_8024924dup , CM000679.1:g.8024922_8024924dup	GRCh37
NC_000017.9:g.7965647_7965649dup	NCBI36
NG_015807.1:g.2313_2315dup
NG_015816.1:g.7489_7491dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.660_662dup MANE Select	ENSP00000446205.2:p.Pro221_Pro222insPro
ENST00000317814.8:c.645_647dup	ENSP00000314774.4:p.Pro216_Pro217insPro
ENST00000541682.6:c.660_662dup	ENSP00000446205.2:p.Pro221_Pro222insPro
NM_001165967.1:c.660_662dup	NP_001159439.1:p.Pro221_Pro222insPro
NM_032580.3:c.645_647dup	NP_115969.2:p.Pro216_Pro217insPro
XM_011524038.1:c.765_767dup	XP_011522340.1:p.Pro256_Pro257insPro
XM_011524039.1:c.756_758dup	XP_011522341.1:p.Pro253_Pro254insPro
XM_011524040.1:c.756_758dup	XP_011522342.1:p.Pro253_Pro254insPro
XM_011524041.1:c.747_749dup	XP_011522343.1:p.Pro250_Pro251insPro
XM_011524042.1:c.618_620dup	XP_011522344.1:p.Pro207_Pro208insPro
XR_934203.1:n.69+1790_69+1792dup
XM_017025232.1:c.765_767dup	XP_016880721.1:p.Pro256_Pro257insPro
XM_024451007.1:c.765_767dup	XP_024306775.1:p.Pro256_Pro257insPro
NM_001165967.2:c.660_662dup MANE Select	NP_001159439.1:p.Pro221_Pro222insPro
NM_032580.4:c.645_647dup	NP_115969.2:p.Pro216_Pro217insPro