Canonical Allele Identifier: CA397987726

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8025059T>G (hg19) ; chr17:g.8121741T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121741T>G , CM000679.2:g.8121741T>G	GRCh38
NC_000017.10:g.8025059T>G , CM000679.1:g.8025059T>G	GRCh37
NC_000017.9:g.7965784T>G	NCBI36
NG_015807.1:g.2176A>C
NG_015816.1:g.7352A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.523A>C MANE Select	ENSP00000446205.2:p.Ser175Arg
ENST00000317814.8:c.508A>C	ENSP00000314774.4:p.Ser170Arg
ENST00000541682.6:c.523A>C	ENSP00000446205.2:p.Ser175Arg
NM_001165967.1:c.523A>C	NP_001159439.1:p.Ser175Arg
NM_032580.3:c.508A>C	NP_115969.2:p.Ser170Arg
XM_011524038.1:c.628A>C	XP_011522340.1:p.Ser210Arg
XM_011524039.1:c.619A>C	XP_011522341.1:p.Ser207Arg
XM_011524040.1:c.619A>C	XP_011522342.1:p.Ser207Arg
XM_011524041.1:c.610A>C	XP_011522343.1:p.Ser204Arg
XM_011524042.1:c.481A>C	XP_011522344.1:p.Ser161Arg
XR_934203.1:n.69+1927T>G
XM_017025232.1:c.628A>C	XP_016880721.1:p.Ser210Arg
XM_024451007.1:c.628A>C	XP_024306775.1:p.Ser210Arg
NM_001165967.2:c.523A>C MANE Select	NP_001159439.1:p.Ser175Arg
NM_032580.4:c.508A>C	NP_115969.2:p.Ser170Arg