Canonical Allele Identifier: CA497955216

Gene: HES7

Linked Data

• gnomAD v4: 17-8121796-T-C
• MyVariant Identifiers: chr17:g.8025114T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121796T>C , CM000679.2:g.8121796T>C	GRCh38
NC_000017.10:g.8025114T>C , CM000679.1:g.8025114T>C	GRCh37
NC_000017.9:g.7965839T>C	NCBI36
NG_015807.1:g.2121A>G
NG_015816.1:g.7297A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.468A>G MANE Select	ENSP00000446205.2:p.Ala156=
ENST00000317814.8:c.453A>G	ENSP00000314774.4:p.Ala151=
ENST00000541682.6:c.468A>G	ENSP00000446205.2:p.Ala156=
NM_001165967.1:c.468A>G	NP_001159439.1:p.Ala156=
NM_032580.3:c.453A>G	NP_115969.2:p.Ala151=
XM_011524038.1:c.573A>G	XP_011522340.1:p.Ala191=
XM_011524039.1:c.564A>G	XP_011522341.1:p.Ala188=
XM_011524040.1:c.564A>G	XP_011522342.1:p.Ala188=
XM_011524041.1:c.555A>G	XP_011522343.1:p.Ala185=
XM_011524042.1:c.426A>G	XP_011522344.1:p.Ala142=
XR_934203.1:n.69+1982T>C
XM_017025232.1:c.573A>G	XP_016880721.1:p.Ala191=
XM_024451007.1:c.573A>G	XP_024306775.1:p.Ala191=
NM_001165967.2:c.468A>G MANE Select	NP_001159439.1:p.Ala156=
NM_032580.4:c.453A>G	NP_115969.2:p.Ala151=