Canonical Allele Identifier: CA397988530

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8025233G>C (hg19) ; chr17:g.8121915G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121915G>C , CM000679.2:g.8121915G>C	GRCh38
NC_000017.10:g.8025233G>C , CM000679.1:g.8025233G>C	GRCh37
NC_000017.9:g.7965958G>C	NCBI36
NG_015807.1:g.2002C>G
NG_015816.1:g.7178C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.349C>G MANE Select	ENSP00000446205.2:p.Pro117Ala
ENST00000317814.8:c.334C>G	ENSP00000314774.4:p.Pro112Ala
ENST00000541682.6:c.349C>G	ENSP00000446205.2:p.Pro117Ala
ENST00000577735.1:c.325C>G	ENSP00000462491.1:p.Pro109Ala
NM_001165967.1:c.349C>G	NP_001159439.1:p.Pro117Ala
NM_032580.3:c.334C>G	NP_115969.2:p.Pro112Ala
XM_011524038.1:c.454C>G	XP_011522340.1:p.Pro152Ala
XM_011524039.1:c.445C>G	XP_011522341.1:p.Pro149Ala
XM_011524040.1:c.445C>G	XP_011522342.1:p.Pro149Ala
XM_011524041.1:c.436C>G	XP_011522343.1:p.Pro146Ala
XM_011524042.1:c.307C>G	XP_011522344.1:p.Pro103Ala
XR_934203.1:n.69+2101G>C
XM_017025232.1:c.454C>G	XP_016880721.1:p.Pro152Ala
XM_024451007.1:c.454C>G	XP_024306775.1:p.Pro152Ala
NM_001165967.2:c.349C>G MANE Select	NP_001159439.1:p.Pro117Ala
NM_032580.4:c.334C>G	NP_115969.2:p.Pro112Ala