Canonical Allele Identifier: CA397988673

Gene: HES7

Linked Data

• gnomAD v4: 17-8121948-G-T
• MyVariant Identifiers: chr17:g.8025266G>T (hg19) ; chr17:g.8121948G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121948G>T , CM000679.2:g.8121948G>T	GRCh38
NC_000017.10:g.8025266G>T , CM000679.1:g.8025266G>T	GRCh37
NC_000017.9:g.7965991G>T	NCBI36
NG_015807.1:g.1969C>A
NG_015816.1:g.7145C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.316C>A MANE Select	ENSP00000446205.2:p.Leu106Ile
ENST00000317814.8:c.301C>A	ENSP00000314774.4:p.Leu101Ile
ENST00000541682.6:c.316C>A	ENSP00000446205.2:p.Leu106Ile
ENST00000577735.1:c.292C>A	ENSP00000462491.1:p.Leu98Ile
NM_001165967.1:c.316C>A	NP_001159439.1:p.Leu106Ile
NM_032580.3:c.301C>A	NP_115969.2:p.Leu101Ile
XM_011524038.1:c.421C>A	XP_011522340.1:p.Leu141Ile
XM_011524039.1:c.412C>A	XP_011522341.1:p.Leu138Ile
XM_011524040.1:c.412C>A	XP_011522342.1:p.Leu138Ile
XM_011524041.1:c.403C>A	XP_011522343.1:p.Leu135Ile
XM_011524042.1:c.274C>A	XP_011522344.1:p.Leu92Ile
XR_934203.1:n.69+2134G>T
XM_017025232.1:c.421C>A	XP_016880721.1:p.Leu141Ile
XM_024451007.1:c.421C>A	XP_024306775.1:p.Leu141Ile
NM_001165967.2:c.316C>A MANE Select	NP_001159439.1:p.Leu106Ile
NM_032580.4:c.301C>A	NP_115969.2:p.Leu101Ile