Canonical Allele Identifier: CA497955513

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8025261G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121943G>C , CM000679.2:g.8121943G>C	GRCh38
NC_000017.10:g.8025261G>C , CM000679.1:g.8025261G>C	GRCh37
NC_000017.9:g.7965986G>C	NCBI36
NG_015807.1:g.1974C>G
NG_015816.1:g.7150C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.321C>G MANE Select	ENSP00000446205.2:p.Arg107=
ENST00000317814.8:c.306C>G	ENSP00000314774.4:p.Arg102=
ENST00000541682.6:c.321C>G	ENSP00000446205.2:p.Arg107=
ENST00000577735.1:c.297C>G	ENSP00000462491.1:p.Arg99=
NM_001165967.1:c.321C>G	NP_001159439.1:p.Arg107=
NM_032580.3:c.306C>G	NP_115969.2:p.Arg102=
XM_011524038.1:c.426C>G	XP_011522340.1:p.Arg142=
XM_011524039.1:c.417C>G	XP_011522341.1:p.Arg139=
XM_011524040.1:c.417C>G	XP_011522342.1:p.Arg139=
XM_011524041.1:c.408C>G	XP_011522343.1:p.Arg136=
XM_011524042.1:c.279C>G	XP_011522344.1:p.Arg93=
XR_934203.1:n.69+2129G>C
XM_017025232.1:c.426C>G	XP_016880721.1:p.Arg142=
XM_024451007.1:c.426C>G	XP_024306775.1:p.Arg142=
NM_001165967.2:c.321C>G MANE Select	NP_001159439.1:p.Arg107=
NM_032580.4:c.306C>G	NP_115969.2:p.Arg102=