Canonical Allele Identifier: CA2576161669

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121649_8121657dup , CM000679.2:g.8121649_8121657dup	GRCh38
NC_000017.10:g.8024967_8024975dup , CM000679.1:g.8024967_8024975dup	GRCh37
NC_000017.9:g.7965692_7965700dup	NCBI36
NG_015807.1:g.2268_2276dup
NG_015816.1:g.7444_7452dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.615_623dup MANE Select	ENSP00000446205.2:p.Pro208_His209insProProPro
ENST00000317814.8:c.600_608dup	ENSP00000314774.4:p.Pro203_His204insProProPro
ENST00000541682.6:c.615_623dup	ENSP00000446205.2:p.Pro208_His209insProProPro
NM_001165967.1:c.615_623dup	NP_001159439.1:p.Pro208_His209insProProPro
NM_032580.3:c.600_608dup	NP_115969.2:p.Pro203_His204insProProPro
XM_011524038.1:c.720_728dup	XP_011522340.1:p.Pro243_His244insProProPro
XM_011524039.1:c.711_719dup	XP_011522341.1:p.Pro240_His241insProProPro
XM_011524040.1:c.711_719dup	XP_011522342.1:p.Pro240_His241insProProPro
XM_011524041.1:c.702_710dup	XP_011522343.1:p.Pro237_His238insProProPro
XM_011524042.1:c.573_581dup	XP_011522344.1:p.Pro194_His195insProProPro
XR_934203.1:n.69+1835_69+1843dup
XM_017025232.1:c.720_728dup	XP_016880721.1:p.Pro243_His244insProProPro
XM_024451007.1:c.720_728dup	XP_024306775.1:p.Pro243_His244insProProPro
NM_001165967.2:c.615_623dup MANE Select	NP_001159439.1:p.Pro208_His209insProProPro
NM_032580.4:c.600_608dup	NP_115969.2:p.Pro203_His204insProProPro