Canonical Allele Identifier: CA2246160251

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121759_8121761delinsCTG , CM000679.2:g.8121759_8121761delinsCTG	GRCh38
NC_000017.10:g.8025077_8025079delinsCTG , CM000679.1:g.8025077_8025079delinsCTG	GRCh37
NC_000017.9:g.7965802_7965804delinsCTG	NCBI36
NG_015807.1:g.2156_2158delinsCAG
NG_015816.1:g.7332_7334delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.503_505delinsCAG MANE Select	ENSP00000446205.2:p.Pro168=
ENST00000317814.8:c.488_490delinsCAG	ENSP00000314774.4:p.Pro163=
ENST00000541682.6:c.503_505delinsCAG	ENSP00000446205.2:p.Pro168=
NM_001165967.1:c.503_505delinsCAG	NP_001159439.1:p.Pro168=
NM_032580.3:c.488_490delinsCAG	NP_115969.2:p.Pro163=
XM_011524038.1:c.608_610delinsCAG	XP_011522340.1:p.Pro203=
XM_011524039.1:c.599_601delinsCAG	XP_011522341.1:p.Pro200=
XM_011524040.1:c.599_601delinsCAG	XP_011522342.1:p.Pro200=
XM_011524041.1:c.590_592delinsCAG	XP_011522343.1:p.Pro197=
XM_011524042.1:c.461_463delinsCAG	XP_011522344.1:p.Pro154=
XR_934203.1:n.69+1945_69+1947delinsCTG
XM_017025232.1:c.608_610delinsCAG	XP_016880721.1:p.Pro203=
XM_024451007.1:c.608_610delinsCAG	XP_024306775.1:p.Pro203=
NM_001165967.2:c.503_505delinsCAG MANE Select	NP_001159439.1:p.Pro168=
NM_032580.4:c.488_490delinsCAG	NP_115969.2:p.Pro163=