Canonical Allele Identifier: CA397989084

Gene: HES7

Linked Data

• gnomAD v4: 17-8122023-C-A
• MyVariant Identifiers: chr17:g.8025341C>A (hg19) ; chr17:g.8122023C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122023C>A , CM000679.2:g.8122023C>A	GRCh38
NC_000017.10:g.8025341C>A , CM000679.1:g.8025341C>A	GRCh37
NC_000017.9:g.7966066C>A	NCBI36
NG_015807.1:g.1894G>T
NG_015816.1:g.7070G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.241G>T MANE Select	ENSP00000446205.2:p.Gly81Trp
ENST00000317814.8:c.227-1G>T	ENSP00000314774.4:n.227-1G>T
ENST00000541682.6:c.241G>T	ENSP00000446205.2:p.Gly81Trp
ENST00000577735.1:c.217G>T	ENSP00000462491.1:p.Gly73Trp
NM_001165967.1:c.241G>T	NP_001159439.1:p.Gly81Trp
NM_032580.3:c.227-1G>T	NP_115969.2:n.227-1G>T
XM_011524038.1:c.346G>T	XP_011522340.1:p.Gly116Trp
XM_011524039.1:c.337G>T	XP_011522341.1:p.Gly113Trp
XM_011524040.1:c.337G>T	XP_011522342.1:p.Gly113Trp
XM_011524041.1:c.328G>T	XP_011522343.1:p.Gly110Trp
XM_011524042.1:c.199G>T	XP_011522344.1:p.Gly67Trp
XR_934203.1:n.69+2209C>A
XM_017025232.1:c.346G>T	XP_016880721.1:p.Gly116Trp
XM_024451007.1:c.346G>T	XP_024306775.1:p.Gly116Trp
NM_001165967.2:c.241G>T MANE Select	NP_001159439.1:p.Gly81Trp
NM_032580.4:c.227-1G>T	NP_115969.2:n.227-1G>T