Canonical Allele Identifier: CA2246159882

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121631T= , CM000679.2:g.8121631T=	GRCh38
NC_000017.10:g.8024949T= , CM000679.1:g.8024949T=	GRCh37
NC_000017.9:g.7965674T=	NCBI36
NG_015807.1:g.2286A=
NG_015816.1:g.7462A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.633A= MANE Select	ENSP00000446205.2:p.Gln211=
ENST00000317814.8:c.618A=	ENSP00000314774.4:p.Gln206=
ENST00000541682.6:c.633A=	ENSP00000446205.2:p.Gln211=
NM_001165967.1:c.633A=	NP_001159439.1:p.Gln211=
NM_032580.3:c.618A=	NP_115969.2:p.Gln206=
XM_011524038.1:c.738A=	XP_011522340.1:p.Gln246=
XM_011524039.1:c.729A=	XP_011522341.1:p.Gln243=
XM_011524040.1:c.729A=	XP_011522342.1:p.Gln243=
XM_011524041.1:c.720A=	XP_011522343.1:p.Gln240=
XM_011524042.1:c.591A=	XP_011522344.1:p.Gln197=
XR_934203.1:n.69+1817T=
XM_017025232.1:c.738A=	XP_016880721.1:p.Gln246=
XM_024451007.1:c.738A=	XP_024306775.1:p.Gln246=
NM_001165967.2:c.633A= MANE Select	NP_001159439.1:p.Gln211=
NM_032580.4:c.618A=	NP_115969.2:p.Gln206=