Canonical Allele Identifier: CA497760860

Gene: HES7

Linked Data

• gnomAD v4: 17-8121676-C-T
• MyVariant Identifiers: chr17:g.8024994C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121676C>T , CM000679.2:g.8121676C>T	GRCh38
NC_000017.10:g.8024994C>T , CM000679.1:g.8024994C>T	GRCh37
NC_000017.9:g.7965719C>T	NCBI36
NG_015807.1:g.2241G>A
NG_015816.1:g.7417G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.588G>A MANE Select	ENSP00000446205.2:p.Ala196=
ENST00000317814.8:c.573G>A	ENSP00000314774.4:p.Ala191=
ENST00000541682.6:c.588G>A	ENSP00000446205.2:p.Ala196=
NM_001165967.1:c.588G>A	NP_001159439.1:p.Ala196=
NM_032580.3:c.573G>A	NP_115969.2:p.Ala191=
XM_011524038.1:c.693G>A	XP_011522340.1:p.Ala231=
XM_011524039.1:c.684G>A	XP_011522341.1:p.Ala228=
XM_011524040.1:c.684G>A	XP_011522342.1:p.Ala228=
XM_011524041.1:c.675G>A	XP_011522343.1:p.Ala225=
XM_011524042.1:c.546G>A	XP_011522344.1:p.Ala182=
XR_934203.1:n.69+1862C>T
XM_017025232.1:c.693G>A	XP_016880721.1:p.Ala231=
XM_024451007.1:c.693G>A	XP_024306775.1:p.Ala231=
NM_001165967.2:c.588G>A MANE Select	NP_001159439.1:p.Ala196=
NM_032580.4:c.573G>A	NP_115969.2:p.Ala191=