Canonical Allele Identifier: CA397988802

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8025290A>T (hg19) ; chr17:g.8121972A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121972A>T , CM000679.2:g.8121972A>T	GRCh38
NC_000017.10:g.8025290A>T , CM000679.1:g.8025290A>T	GRCh37
NC_000017.9:g.7966015A>T	NCBI36
NG_015807.1:g.1945T>A
NG_015816.1:g.7121T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.292T>A MANE Select	ENSP00000446205.2:p.Leu98Met
ENST00000317814.8:c.277T>A	ENSP00000314774.4:p.Leu93Met
ENST00000541682.6:c.292T>A	ENSP00000446205.2:p.Leu98Met
ENST00000577735.1:c.268T>A	ENSP00000462491.1:p.Leu90Met
NM_001165967.1:c.292T>A	NP_001159439.1:p.Leu98Met
NM_032580.3:c.277T>A	NP_115969.2:p.Leu93Met
XM_011524038.1:c.397T>A	XP_011522340.1:p.Leu133Met
XM_011524039.1:c.388T>A	XP_011522341.1:p.Leu130Met
XM_011524040.1:c.388T>A	XP_011522342.1:p.Leu130Met
XM_011524041.1:c.379T>A	XP_011522343.1:p.Leu127Met
XM_011524042.1:c.250T>A	XP_011522344.1:p.Leu84Met
XR_934203.1:n.69+2158A>T
XM_017025232.1:c.397T>A	XP_016880721.1:p.Leu133Met
XM_024451007.1:c.397T>A	XP_024306775.1:p.Leu133Met
NM_001165967.2:c.292T>A MANE Select	NP_001159439.1:p.Leu98Met
NM_032580.4:c.277T>A	NP_115969.2:p.Leu93Met