Canonical Allele Identifier: CA2503925677

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121545A>C , CM000679.2:g.8121545A>C	GRCh38
NC_000017.10:g.8024863A>C , CM000679.1:g.8024863A>C	GRCh37
NC_000017.9:g.7965588A>C	NCBI36
NG_015807.1:g.2372T>G
NG_015816.1:g.7548T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*26T>G MANE Select	ENSP00000446205.2:n.*26T>G
ENST00000541682.6:c.719T>G	ENSP00000446205.2:n.719T>G
NM_001165967.1:c.*26T>G	NP_001159439.1:n.*26T>G
NM_032580.3:c.*26T>G	NP_115969.2:n.*26T>G
XM_011524038.1:c.*26T>G	XP_011522340.1:n.*26T>G
XM_011524039.1:c.*26T>G	XP_011522341.1:n.*26T>G
XM_011524040.1:c.*26T>G	XP_011522342.1:n.*26T>G
XM_011524041.1:c.*26T>G	XP_011522343.1:n.*26T>G
XM_011524042.1:c.*26T>G	XP_011522344.1:n.*26T>G
XR_934203.1:n.69+1731A>C
XM_017025232.1:c.*26T>G	XP_016880721.1:n.*26T>G
XM_024451007.1:c.*26T>G	XP_024306775.1:n.*26T>G
NM_001165967.2:c.*26T>G MANE Select	NP_001159439.1:n.*26T>G
NM_032580.4:c.*26T>G	NP_115969.2:n.*26T>G