Canonical Allele Identifier: CA981238417

Gene: HES7

Linked Data

• dbSNP Id: rs1981319809
• gnomAD v3: 17-8121541-CT-C
• gnomAD v4: 17-8121541-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121542del , CM000679.2:g.8121542del	GRCh38
NC_000017.10:g.8024860del , CM000679.1:g.8024860del	GRCh37
NC_000017.9:g.7965585del	NCBI36
NG_015807.1:g.2375del
NG_015816.1:g.7551del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*29del MANE Select	ENSP00000446205.2:n.*29del
ENST00000541682.6:c.722del	ENSP00000446205.2:n.722del
NM_001165967.1:c.*29del	NP_001159439.1:n.*29del
NM_032580.3:c.*29del	NP_115969.2:n.*29del
XM_011524038.1:c.*29del	XP_011522340.1:n.*29del
XM_011524039.1:c.*29del	XP_011522341.1:n.*29del
XM_011524040.1:c.*29del	XP_011522342.1:n.*29del
XM_011524041.1:c.*29del	XP_011522343.1:n.*29del
XM_011524042.1:c.*29del	XP_011522344.1:n.*29del
XR_934203.1:n.69+1728del
XM_017025232.1:c.*29del	XP_016880721.1:n.*29del
XM_024451007.1:c.*29del	XP_024306775.1:n.*29del
NM_001165967.2:c.*29del MANE Select	NP_001159439.1:n.*29del
NM_032580.4:c.*29del	NP_115969.2:n.*29del