Canonical Allele Identifier: CA287537031

Gene: HES7

Linked Data

• dbSNP Id: rs1038368865
• MyVariant Identifiers: chr17:g.8024995G>C (hg19) ; chr17:g.8121677G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121677G>C , CM000679.2:g.8121677G>C	GRCh38
NC_000017.10:g.8024995G>C , CM000679.1:g.8024995G>C	GRCh37
NC_000017.9:g.7965720G>C	NCBI36
NG_015807.1:g.2240C>G
NG_015816.1:g.7416C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.587C>G MANE Select	ENSP00000446205.2:p.Ala196Gly
ENST00000317814.8:c.572C>G	ENSP00000314774.4:p.Ala191Gly
ENST00000541682.6:c.587C>G	ENSP00000446205.2:p.Ala196Gly
NM_001165967.1:c.587C>G	NP_001159439.1:p.Ala196Gly
NM_032580.3:c.572C>G	NP_115969.2:p.Ala191Gly
XM_011524038.1:c.692C>G	XP_011522340.1:p.Ala231Gly
XM_011524039.1:c.683C>G	XP_011522341.1:p.Ala228Gly
XM_011524040.1:c.683C>G	XP_011522342.1:p.Ala228Gly
XM_011524041.1:c.674C>G	XP_011522343.1:p.Ala225Gly
XM_011524042.1:c.545C>G	XP_011522344.1:p.Ala182Gly
XR_934203.1:n.69+1863G>C
XM_017025232.1:c.692C>G	XP_016880721.1:p.Ala231Gly
XM_024451007.1:c.692C>G	XP_024306775.1:p.Ala231Gly
NM_001165967.2:c.587C>G MANE Select	NP_001159439.1:p.Ala196Gly
NM_032580.4:c.572C>G	NP_115969.2:p.Ala191Gly