Canonical Allele Identifier: CA497955401

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8025318C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122000C>T , CM000679.2:g.8122000C>T	GRCh38
NC_000017.10:g.8025318C>T , CM000679.1:g.8025318C>T	GRCh37
NC_000017.9:g.7966043C>T	NCBI36
NG_015807.1:g.1917G>A
NG_015816.1:g.7093G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.264G>A MANE Select	ENSP00000446205.2:p.Gln88=
ENST00000317814.8:c.249G>A	ENSP00000314774.4:p.Gln83=
ENST00000541682.6:c.264G>A	ENSP00000446205.2:p.Gln88=
ENST00000577735.1:c.240G>A	ENSP00000462491.1:p.Gln80=
NM_001165967.1:c.264G>A	NP_001159439.1:p.Gln88=
NM_032580.3:c.249G>A	NP_115969.2:p.Gln83=
XM_011524038.1:c.369G>A	XP_011522340.1:p.Gln123=
XM_011524039.1:c.360G>A	XP_011522341.1:p.Gln120=
XM_011524040.1:c.360G>A	XP_011522342.1:p.Gln120=
XM_011524041.1:c.351G>A	XP_011522343.1:p.Gln117=
XM_011524042.1:c.222G>A	XP_011522344.1:p.Gln74=
XR_934203.1:n.69+2186C>T
XM_017025232.1:c.369G>A	XP_016880721.1:p.Gln123=
XM_024451007.1:c.369G>A	XP_024306775.1:p.Gln123=
NM_001165967.2:c.264G>A MANE Select	NP_001159439.1:p.Gln88=
NM_032580.4:c.249G>A	NP_115969.2:p.Gln83=