Canonical Allele Identifier: CA397988665

Gene: HES7

Linked Data

• gnomAD v4: 17-8121947-A-T
• MyVariant Identifiers: chr17:g.8025265A>T (hg19) ; chr17:g.8121947A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121947A>T , CM000679.2:g.8121947A>T	GRCh38
NC_000017.10:g.8025265A>T , CM000679.1:g.8025265A>T	GRCh37
NC_000017.9:g.7965990A>T	NCBI36
NG_015807.1:g.1970T>A
NG_015816.1:g.7146T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.317T>A MANE Select	ENSP00000446205.2:p.Leu106His
ENST00000317814.8:c.302T>A	ENSP00000314774.4:p.Leu101His
ENST00000541682.6:c.317T>A	ENSP00000446205.2:p.Leu106His
ENST00000577735.1:c.293T>A	ENSP00000462491.1:p.Leu98His
NM_001165967.1:c.317T>A	NP_001159439.1:p.Leu106His
NM_032580.3:c.302T>A	NP_115969.2:p.Leu101His
XM_011524038.1:c.422T>A	XP_011522340.1:p.Leu141His
XM_011524039.1:c.413T>A	XP_011522341.1:p.Leu138His
XM_011524040.1:c.413T>A	XP_011522342.1:p.Leu138His
XM_011524041.1:c.404T>A	XP_011522343.1:p.Leu135His
XM_011524042.1:c.275T>A	XP_011522344.1:p.Leu92His
XR_934203.1:n.69+2133A>T
XM_017025232.1:c.422T>A	XP_016880721.1:p.Leu141His
XM_024451007.1:c.422T>A	XP_024306775.1:p.Leu141His
NM_001165967.2:c.317T>A MANE Select	NP_001159439.1:p.Leu106His
NM_032580.4:c.302T>A	NP_115969.2:p.Leu101His