Canonical Allele Identifier: CA497760784

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8024910A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121592A>C , CM000679.2:g.8121592A>C	GRCh38
NC_000017.10:g.8024910A>C , CM000679.1:g.8024910A>C	GRCh37
NC_000017.9:g.7965635A>C	NCBI36
NG_015807.1:g.2325T>G
NG_015816.1:g.7501T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.672T>G MANE Select	ENSP00000446205.2:p.Ala224=
ENST00000317814.8:c.657T>G	ENSP00000314774.4:p.Ala219=
ENST00000541682.6:c.672T>G	ENSP00000446205.2:p.Ala224=
NM_001165967.1:c.672T>G	NP_001159439.1:p.Ala224=
NM_032580.3:c.657T>G	NP_115969.2:p.Ala219=
XM_011524038.1:c.777T>G	XP_011522340.1:p.Ala259=
XM_011524039.1:c.768T>G	XP_011522341.1:p.Ala256=
XM_011524040.1:c.768T>G	XP_011522342.1:p.Ala256=
XM_011524041.1:c.759T>G	XP_011522343.1:p.Ala253=
XM_011524042.1:c.630T>G	XP_011522344.1:p.Ala210=
XR_934203.1:n.69+1778A>C
XM_017025232.1:c.777T>G	XP_016880721.1:p.Ala259=
XM_024451007.1:c.777T>G	XP_024306775.1:p.Ala259=
NM_001165967.2:c.672T>G MANE Select	NP_001159439.1:p.Ala224=
NM_032580.4:c.657T>G	NP_115969.2:p.Ala219=