Canonical Allele Identifier: CA2246160966

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122044_8122068delinsCGGCCGGCGGGAGCACAGGTGGGCA , CM000679.2:g.8122044_8122068delinsCGGCCGGCGGGAGCACAGGTGGGCA	GRCh38
NC_000017.10:g.8025362_8025386delinsCGGCCGGCGGGAGCACAGGTGGGCA , CM000679.1:g.8025362_8025386delinsCGGCCGGCGGGAGCACAGGTGGGCA	GRCh37
NC_000017.9:g.7966087_7966111delinsCGGCCGGCGGGAGCACAGGTGGGCA	NCBI36
NG_015807.1:g.1849_1873delinsTGCCCACCTGTGCTCCCGCCGGCCG
NG_015816.1:g.7025_7049delinsTGCCCACCTGTGCTCCCGCCGGCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.227-31_227-7delinsTGCCCACCTGTGCTCCCGCCGGCCG MANE Select	ENSP00000446205.2:n.227-31_227-7delinsTGCCCACCTGTGCTCCCGCCGGC...
ENST00000317814.8:c.227-46_227-22delinsTGCCCACCTGTGCTCCCGCCGGCCG	ENSP00000314774.4:n.227-46_227-22delinsTGCCCACCTGTGCTCCCGCCGG...
ENST00000541682.6:c.227-31_227-7delinsTGCCCACCTGTGCTCCCGCCGGCCG	ENSP00000446205.2:n.227-31_227-7delinsTGCCCACCTGTGCTCCCGCCGGC...
ENST00000577735.1:c.203-31_203-7delinsTGCCCACCTGTGCTCCCGCCGGCCG	ENSP00000462491.1:n.203-31_203-7delinsTGCCCACCTGTGCTCCCGCCGGC...
NM_001165967.1:c.227-31_227-7delinsTGCCCACCTGTGCTCCCGCCGGCCG	NP_001159439.1:n.227-31_227-7delinsTGCCCACCTGTGCTCCCGCCGGCCG
NM_032580.3:c.227-46_227-22delinsTGCCCACCTGTGCTCCCGCCGGCCG	NP_115969.2:n.227-46_227-22delinsTGCCCACCTGTGCTCCCGCCGGCCG
XM_011524038.1:c.332-31_332-7delinsTGCCCACCTGTGCTCCCGCCGGCCG	XP_011522340.1:n.332-31_332-7delinsTGCCCACCTGTGCTCCCGCCGGCCG
XM_011524039.1:c.323-31_323-7delinsTGCCCACCTGTGCTCCCGCCGGCCG	XP_011522341.1:n.323-31_323-7delinsTGCCCACCTGTGCTCCCGCCGGCCG
XM_011524040.1:c.323-31_323-7delinsTGCCCACCTGTGCTCCCGCCGGCCG	XP_011522342.1:n.323-31_323-7delinsTGCCCACCTGTGCTCCCGCCGGCCG
XM_011524041.1:c.314-31_314-7delinsTGCCCACCTGTGCTCCCGCCGGCCG	XP_011522343.1:n.314-31_314-7delinsTGCCCACCTGTGCTCCCGCCGGCCG
XM_011524042.1:c.185-31_185-7delinsTGCCCACCTGTGCTCCCGCCGGCCG	XP_011522344.1:n.185-31_185-7delinsTGCCCACCTGTGCTCCCGCCGGCCG
XR_934203.1:n.69+2230_69+2254delinsCGGCCGGCGGGAGCACAGGTGGGCA
XM_017025232.1:c.332-31_332-7delinsTGCCCACCTGTGCTCCCGCCGGCCG	XP_016880721.1:n.332-31_332-7delinsTGCCCACCTGTGCTCCCGCCGGCCG
XM_024451007.1:c.332-31_332-7delinsTGCCCACCTGTGCTCCCGCCGGCCG	XP_024306775.1:n.332-31_332-7delinsTGCCCACCTGTGCTCCCGCCGGCCG
NM_001165967.2:c.227-31_227-7delinsTGCCCACCTGTGCTCCCGCCGGCCG MANE Select	NP_001159439.1:n.227-31_227-7delinsTGCCCACCTGTGCTCCCGCCGGCCG
NM_032580.4:c.227-46_227-22delinsTGCCCACCTGTGCTCCCGCCGGCCG	NP_115969.2:n.227-46_227-22delinsTGCCCACCTGTGCTCCCGCCGGCCG