Canonical Allele Identifier: CA497955348

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8025300G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121982G>T , CM000679.2:g.8121982G>T	GRCh38
NC_000017.10:g.8025300G>T , CM000679.1:g.8025300G>T	GRCh37
NC_000017.9:g.7966025G>T	NCBI36
NG_015807.1:g.1935C>A
NG_015816.1:g.7111C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.282C>A MANE Select	ENSP00000446205.2:p.Ala94=
ENST00000317814.8:c.267C>A	ENSP00000314774.4:p.Ala89=
ENST00000541682.6:c.282C>A	ENSP00000446205.2:p.Ala94=
ENST00000577735.1:c.258C>A	ENSP00000462491.1:p.Ala86=
NM_001165967.1:c.282C>A	NP_001159439.1:p.Ala94=
NM_032580.3:c.267C>A	NP_115969.2:p.Ala89=
XM_011524038.1:c.387C>A	XP_011522340.1:p.Ala129=
XM_011524039.1:c.378C>A	XP_011522341.1:p.Ala126=
XM_011524040.1:c.378C>A	XP_011522342.1:p.Ala126=
XM_011524041.1:c.369C>A	XP_011522343.1:p.Ala123=
XM_011524042.1:c.240C>A	XP_011522344.1:p.Ala80=
XR_934203.1:n.69+2168G>T
XM_017025232.1:c.387C>A	XP_016880721.1:p.Ala129=
XM_024451007.1:c.387C>A	XP_024306775.1:p.Ala129=
NM_001165967.2:c.282C>A MANE Select	NP_001159439.1:p.Ala94=
NM_032580.4:c.267C>A	NP_115969.2:p.Ala89=