Canonical Allele Identifier: CA2511739718

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121557_8121558dup , CM000679.2:g.8121557_8121558dup	GRCh38
NC_000017.10:g.8024875_8024876dup , CM000679.1:g.8024875_8024876dup	GRCh37
NC_000017.9:g.7965600_7965601dup	NCBI36
NG_015807.1:g.2359_2360dup
NG_015816.1:g.7535_7536dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*13_*14dup MANE Select	ENSP00000446205.2:n.*13_*14dup
ENST00000541682.6:c.706_707dup	ENSP00000446205.2:n.706_707dup
NM_001165967.1:c.*13_*14dup	NP_001159439.1:n.*13_*14dup
NM_032580.3:c.*13_*14dup	NP_115969.2:n.*13_*14dup
XM_011524038.1:c.*13_*14dup	XP_011522340.1:n.*13_*14dup
XM_011524039.1:c.*13_*14dup	XP_011522341.1:n.*13_*14dup
XM_011524040.1:c.*13_*14dup	XP_011522342.1:n.*13_*14dup
XM_011524041.1:c.*13_*14dup	XP_011522343.1:n.*13_*14dup
XM_011524042.1:c.*13_*14dup	XP_011522344.1:n.*13_*14dup
XR_934203.1:n.69+1743_69+1744dup
XM_017025232.1:c.*13_*14dup	XP_016880721.1:n.*13_*14dup
XM_024451007.1:c.*13_*14dup	XP_024306775.1:n.*13_*14dup
NM_001165967.2:c.*13_*14dup MANE Select	NP_001159439.1:n.*13_*14dup
NM_032580.4:c.*13_*14dup	NP_115969.2:n.*13_*14dup