Canonical Allele Identifier: CA2808397530

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121548C>G , CM000679.2:g.8121548C>G	GRCh38
NC_000017.10:g.8024866C>G , CM000679.1:g.8024866C>G	GRCh37
NC_000017.9:g.7965591C>G	NCBI36
NG_015807.1:g.2369G>C
NG_015816.1:g.7545G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*23G>C MANE Select	ENSP00000446205.2:n.*23G>C
ENST00000541682.6:c.716G>C	ENSP00000446205.2:n.716G>C
NM_001165967.1:c.*23G>C	NP_001159439.1:n.*23G>C
NM_032580.3:c.*23G>C	NP_115969.2:n.*23G>C
XM_011524038.1:c.*23G>C	XP_011522340.1:n.*23G>C
XM_011524039.1:c.*23G>C	XP_011522341.1:n.*23G>C
XM_011524040.1:c.*23G>C	XP_011522342.1:n.*23G>C
XM_011524041.1:c.*23G>C	XP_011522343.1:n.*23G>C
XM_011524042.1:c.*23G>C	XP_011522344.1:n.*23G>C
XR_934203.1:n.69+1734C>G
XM_017025232.1:c.*23G>C	XP_016880721.1:n.*23G>C
XM_024451007.1:c.*23G>C	XP_024306775.1:n.*23G>C
NM_001165967.2:c.*23G>C MANE Select	NP_001159439.1:n.*23G>C
NM_032580.4:c.*23G>C	NP_115969.2:n.*23G>C