Canonical Allele Identifier: CA397986936

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8024912C>G (hg19) ; chr17:g.8121594C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121594C>G , CM000679.2:g.8121594C>G	GRCh38
NC_000017.10:g.8024912C>G , CM000679.1:g.8024912C>G	GRCh37
NC_000017.9:g.7965637C>G	NCBI36
NG_015807.1:g.2323G>C
NG_015816.1:g.7499G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.670G>C MANE Select	ENSP00000446205.2:p.Ala224Pro
ENST00000317814.8:c.655G>C	ENSP00000314774.4:p.Ala219Pro
ENST00000541682.6:c.670G>C	ENSP00000446205.2:p.Ala224Pro
NM_001165967.1:c.670G>C	NP_001159439.1:p.Ala224Pro
NM_032580.3:c.655G>C	NP_115969.2:p.Ala219Pro
XM_011524038.1:c.775G>C	XP_011522340.1:p.Ala259Pro
XM_011524039.1:c.766G>C	XP_011522341.1:p.Ala256Pro
XM_011524040.1:c.766G>C	XP_011522342.1:p.Ala256Pro
XM_011524041.1:c.757G>C	XP_011522343.1:p.Ala253Pro
XM_011524042.1:c.628G>C	XP_011522344.1:p.Ala210Pro
XR_934203.1:n.69+1780C>G
XM_017025232.1:c.775G>C	XP_016880721.1:p.Ala259Pro
XM_024451007.1:c.775G>C	XP_024306775.1:p.Ala259Pro
NM_001165967.2:c.670G>C MANE Select	NP_001159439.1:p.Ala224Pro
NM_032580.4:c.655G>C	NP_115969.2:p.Ala219Pro