Canonical Allele Identifier: CA2246157945

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8120724_8120726delinsCCT , CM000679.2:g.8120724_8120726delinsCCT	GRCh38
NC_000017.10:g.8024042_8024044delinsCCT , CM000679.1:g.8024042_8024044delinsCCT	GRCh37
NC_000017.9:g.7964767_7964769delinsCCT	NCBI36
NG_015807.1:g.3191_3193delinsAGG
NG_015816.1:g.8367_8369delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*845_*847delinsAGG MANE Select	ENSP00000446205.2:n.*845_*847delinsAGG
ENST00000541682.6:c.1538_1540delinsAGG	ENSP00000446205.2:n.1538_1540delinsAGG
NM_001165967.1:c.*845_*847delinsAGG	NP_001159439.1:n.*845_*847delinsAGG
NM_032580.3:c.*845_*847delinsAGG	NP_115969.2:n.*845_*847delinsAGG
XM_011524038.1:c.*845_*847delinsAGG	XP_011522340.1:n.*845_*847delinsAGG
XR_934203.1:n.69+910_69+912delinsCCT
XM_017025232.1:c.*845_*847delinsAGG	XP_016880721.1:n.*845_*847delinsAGG
XM_024451007.1:c.*845_*847delinsAGG	XP_024306775.1:n.*845_*847delinsAGG
NM_001165967.2:c.*845_*847delinsAGG MANE Select	NP_001159439.1:n.*845_*847delinsAGG
NM_032580.4:c.*845_*847delinsAGG	NP_115969.2:n.*845_*847delinsAGG