Canonical Allele Identifier: CA775622990

Gene: HES7

Linked Data

• dbSNP Id: rs1450989137
• MyVariant Identifiers: chr17:g.8024877_8024878insCCC (hg19) ; chr17:g.8121559_8121560insCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121563_8121565dup , CM000679.2:g.8121563_8121565dup	GRCh38
NC_000017.10:g.8024881_8024883dup , CM000679.1:g.8024881_8024883dup	GRCh37
NC_000017.9:g.7965606_7965608dup	NCBI36
NG_015807.1:g.2355_2357dup
NG_015816.1:g.7531_7533dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*9_*11dup MANE Select	ENSP00000446205.2:n.*9_*11dup
ENST00000541682.6:c.702_704dup	ENSP00000446205.2:n.702_704dup
NM_001165967.1:c.*9_*11dup	NP_001159439.1:n.*9_*11dup
NM_032580.3:c.*9_*11dup	NP_115969.2:n.*9_*11dup
XM_011524038.1:c.*9_*11dup	XP_011522340.1:n.*9_*11dup
XM_011524039.1:c.*9_*11dup	XP_011522341.1:n.*9_*11dup
XM_011524040.1:c.*9_*11dup	XP_011522342.1:n.*9_*11dup
XM_011524041.1:c.*9_*11dup	XP_011522343.1:n.*9_*11dup
XM_011524042.1:c.*9_*11dup	XP_011522344.1:n.*9_*11dup
XR_934203.1:n.69+1749_69+1751dup
XM_017025232.1:c.*9_*11dup	XP_016880721.1:n.*9_*11dup
XM_024451007.1:c.*9_*11dup	XP_024306775.1:n.*9_*11dup
NM_001165967.2:c.*9_*11dup MANE Select	NP_001159439.1:n.*9_*11dup
NM_032580.4:c.*9_*11dup	NP_115969.2:n.*9_*11dup