Canonical Allele Identifier: CA497955514

Gene: HES7

Linked Data

• gnomAD v4: 17-8121943-G-T
• MyVariant Identifiers: chr17:g.8025261G>T (hg19)

Genomic Alleles

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

Transcript Alleles

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