Canonical Allele Identifier: CA2590217291

Gene: HES7

Linked Data

• dbSNP Id: rs2151853272
• gnomAD v3: 17-8121542-TA-T
• gnomAD v4: 17-8121542-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121543del , CM000679.2:g.8121543del	GRCh38
NC_000017.10:g.8024861del , CM000679.1:g.8024861del	GRCh37
NC_000017.9:g.7965586del	NCBI36
NG_015807.1:g.2374del
NG_015816.1:g.7550del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*28del MANE Select	ENSP00000446205.2:n.*28del
ENST00000541682.6:c.721del	ENSP00000446205.2:n.721del
NM_001165967.1:c.*28del	NP_001159439.1:n.*28del
NM_032580.3:c.*28del	NP_115969.2:n.*28del
XM_011524038.1:c.*28del	XP_011522340.1:n.*28del
XM_011524039.1:c.*28del	XP_011522341.1:n.*28del
XM_011524040.1:c.*28del	XP_011522342.1:n.*28del
XM_011524041.1:c.*28del	XP_011522343.1:n.*28del
XM_011524042.1:c.*28del	XP_011522344.1:n.*28del
XR_934203.1:n.69+1729del
XM_017025232.1:c.*28del	XP_016880721.1:n.*28del
XM_024451007.1:c.*28del	XP_024306775.1:n.*28del
NM_001165967.2:c.*28del MANE Select	NP_001159439.1:n.*28del
NM_032580.4:c.*28del	NP_115969.2:n.*28del