Canonical Allele Identifier: CA497760838

Gene: HES7

Linked Data

• dbSNP Id: rs1981330038
• gnomAD v4: 17-8121655-C-T
• MyVariant Identifiers: chr17:g.8024973C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121655C>T , CM000679.2:g.8121655C>T	GRCh38
NC_000017.10:g.8024973C>T , CM000679.1:g.8024973C>T	GRCh37
NC_000017.9:g.7965698C>T	NCBI36
NG_015807.1:g.2262G>A
NG_015816.1:g.7438G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.609G>A MANE Select	ENSP00000446205.2:p.Pro203=
ENST00000317814.8:c.594G>A	ENSP00000314774.4:p.Pro198=
ENST00000541682.6:c.609G>A	ENSP00000446205.2:p.Pro203=
NM_001165967.1:c.609G>A	NP_001159439.1:p.Pro203=
NM_032580.3:c.594G>A	NP_115969.2:p.Pro198=
XM_011524038.1:c.714G>A	XP_011522340.1:p.Pro238=
XM_011524039.1:c.705G>A	XP_011522341.1:p.Pro235=
XM_011524040.1:c.705G>A	XP_011522342.1:p.Pro235=
XM_011524041.1:c.696G>A	XP_011522343.1:p.Pro232=
XM_011524042.1:c.567G>A	XP_011522344.1:p.Pro189=
XR_934203.1:n.69+1841C>T
XM_017025232.1:c.714G>A	XP_016880721.1:p.Pro238=
XM_024451007.1:c.714G>A	XP_024306775.1:p.Pro238=
NM_001165967.2:c.609G>A MANE Select	NP_001159439.1:p.Pro203=
NM_032580.4:c.594G>A	NP_115969.2:p.Pro198=