Canonical Allele Identifier: CA397988853

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8025299T>G (hg19) ; chr17:g.8121981T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121981T>G , CM000679.2:g.8121981T>G	GRCh38
NC_000017.10:g.8025299T>G , CM000679.1:g.8025299T>G	GRCh37
NC_000017.9:g.7966024T>G	NCBI36
NG_015807.1:g.1936A>C
NG_015816.1:g.7112A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.283A>C MANE Select	ENSP00000446205.2:p.Ser95Arg
ENST00000317814.8:c.268A>C	ENSP00000314774.4:p.Ser90Arg
ENST00000541682.6:c.283A>C	ENSP00000446205.2:p.Ser95Arg
ENST00000577735.1:c.259A>C	ENSP00000462491.1:p.Ser87Arg
NM_001165967.1:c.283A>C	NP_001159439.1:p.Ser95Arg
NM_032580.3:c.268A>C	NP_115969.2:p.Ser90Arg
XM_011524038.1:c.388A>C	XP_011522340.1:p.Ser130Arg
XM_011524039.1:c.379A>C	XP_011522341.1:p.Ser127Arg
XM_011524040.1:c.379A>C	XP_011522342.1:p.Ser127Arg
XM_011524041.1:c.370A>C	XP_011522343.1:p.Ser124Arg
XM_011524042.1:c.241A>C	XP_011522344.1:p.Ser81Arg
XR_934203.1:n.69+2167T>G
XM_017025232.1:c.388A>C	XP_016880721.1:p.Ser130Arg
XM_024451007.1:c.388A>C	XP_024306775.1:p.Ser130Arg
NM_001165967.2:c.283A>C MANE Select	NP_001159439.1:p.Ser95Arg
NM_032580.4:c.268A>C	NP_115969.2:p.Ser90Arg