Canonical Allele Identifier: CA497761886

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8123040G>C , CM000679.2:g.8123040G>C	GRCh38
NC_000017.10:g.8026358G>C , CM000679.1:g.8026358G>C	GRCh37
NC_000017.9:g.7967083G>C	NCBI36
NG_015807.1:g.877C>G
NG_015816.1:g.6053C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001165967.2:c.129C>G MANE Select	NP_001159439.1:p.Thr43=
ENST00000541682.7:c.129C>G MANE Select	ENSP00000446205.2:p.Thr43=
NM_001165967.1:c.129C>G	NP_001159439.1:p.Thr43=
NM_032580.3:c.129C>G	NP_115969.2:p.Thr43=
NM_032580.4:c.129C>G	NP_115969.2:p.Thr43=
ENST00000317814.8:c.129C>G	ENSP00000314774.4:p.Thr43=
ENST00000541682.6:c.129C>G	ENSP00000446205.2:p.Thr43=
ENST00000577735.1:c.105C>G	ENSP00000462491.1:p.Thr35=
XM_011524038.1:c.234C>G	XP_011522340.1:p.Thr78=
XM_011524039.1:c.225C>G	XP_011522341.1:p.Thr75=
XM_011524040.1:c.225C>G	XP_011522342.1:p.Thr75=
XM_011524041.1:c.216C>G	XP_011522343.1:p.Thr72=
XM_011524042.1:c.87C>G	XP_011522344.1:p.Thr29=
XM_017025232.1:c.234C>G	XP_016880721.1:p.Thr78=
XM_024451007.1:c.234C>G	XP_024306775.1:p.Thr78=
XR_934203.1:n.69+3226G>C