Canonical Allele Identifier: CA2246159847

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121618_8121619delinsTG , CM000679.2:g.8121618_8121619delinsTG	GRCh38
NC_000017.10:g.8024936_8024937delinsTG , CM000679.1:g.8024936_8024937delinsTG	GRCh37
NC_000017.9:g.7965661_7965662delinsTG	NCBI36
NG_015807.1:g.2298_2299delinsCA
NG_015816.1:g.7474_7475delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.645_646delinsCA MANE Select	ENSP00000446205.2:p.Pro215=
ENST00000317814.8:c.630_631delinsCA	ENSP00000314774.4:p.Pro210=
ENST00000541682.6:c.645_646delinsCA	ENSP00000446205.2:p.Pro215=
NM_001165967.1:c.645_646delinsCA	NP_001159439.1:p.Pro215=
NM_032580.3:c.630_631delinsCA	NP_115969.2:p.Pro210=
XM_011524038.1:c.750_751delinsCA	XP_011522340.1:p.Pro250=
XM_011524039.1:c.741_742delinsCA	XP_011522341.1:p.Pro247=
XM_011524040.1:c.741_742delinsCA	XP_011522342.1:p.Pro247=
XM_011524041.1:c.732_733delinsCA	XP_011522343.1:p.Pro244=
XM_011524042.1:c.603_604delinsCA	XP_011522344.1:p.Pro201=
XR_934203.1:n.69+1804_69+1805delinsTG
XM_017025232.1:c.750_751delinsCA	XP_016880721.1:p.Pro250=
XM_024451007.1:c.750_751delinsCA	XP_024306775.1:p.Pro250=
NM_001165967.2:c.645_646delinsCA MANE Select	NP_001159439.1:p.Pro215=
NM_032580.4:c.630_631delinsCA	NP_115969.2:p.Pro210=