Canonical Allele Identifier: CA2499889507

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121564C>T , CM000679.2:g.8121564C>T	GRCh38
NC_000017.10:g.8024882C>T , CM000679.1:g.8024882C>T	GRCh37
NC_000017.9:g.7965607C>T	NCBI36
NG_015807.1:g.2353G>A
NG_015816.1:g.7529G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*7G>A MANE Select	ENSP00000446205.2:n.*7G>A
ENST00000541682.6:c.700G>A	ENSP00000446205.2:n.700G>A
NM_001165967.1:c.*7G>A	NP_001159439.1:n.*7G>A
NM_032580.3:c.*7G>A	NP_115969.2:n.*7G>A
XM_011524038.1:c.*7G>A	XP_011522340.1:n.*7G>A
XM_011524039.1:c.*7G>A	XP_011522341.1:n.*7G>A
XM_011524040.1:c.*7G>A	XP_011522342.1:n.*7G>A
XM_011524041.1:c.*7G>A	XP_011522343.1:n.*7G>A
XM_011524042.1:c.*7G>A	XP_011522344.1:n.*7G>A
XR_934203.1:n.69+1750C>T
XM_017025232.1:c.*7G>A	XP_016880721.1:n.*7G>A
XM_024451007.1:c.*7G>A	XP_024306775.1:n.*7G>A
NM_001165967.2:c.*7G>A MANE Select	NP_001159439.1:n.*7G>A
NM_032580.4:c.*7G>A	NP_115969.2:n.*7G>A