Canonical Allele Identifier: CA2635936393

Gene: HES7

Linked Data

• gnomAD v4: 17-8121526-GTCTCTACCCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121527_8121536del , CM000679.2:g.8121527_8121536del	GRCh38
NC_000017.10:g.8024845_8024854del , CM000679.1:g.8024845_8024854del	GRCh37
NC_000017.9:g.7965570_7965579del	NCBI36
NG_015807.1:g.2381_2390del
NG_015816.1:g.7557_7566del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*35_*44del MANE Select	ENSP00000446205.2:n.*35_*44del
ENST00000541682.6:c.728_737del	ENSP00000446205.2:n.728_737del
NM_001165967.1:c.*35_*44del	NP_001159439.1:n.*35_*44del
NM_032580.3:c.*35_*44del	NP_115969.2:n.*35_*44del
XM_011524038.1:c.*35_*44del	XP_011522340.1:n.*35_*44del
XM_011524039.1:c.*35_*44del	XP_011522341.1:n.*35_*44del
XM_011524040.1:c.*35_*44del	XP_011522342.1:n.*35_*44del
XM_011524041.1:c.*35_*44del	XP_011522343.1:n.*35_*44del
XM_011524042.1:c.*35_*44del	XP_011522344.1:n.*35_*44del
XR_934203.1:n.69+1713_69+1722del
XM_017025232.1:c.*35_*44del	XP_016880721.1:n.*35_*44del
XM_024451007.1:c.*35_*44del	XP_024306775.1:n.*35_*44del
NM_001165967.2:c.*35_*44del MANE Select	NP_001159439.1:n.*35_*44del
NM_032580.4:c.*35_*44del	NP_115969.2:n.*35_*44del