Canonical Allele Identifier: CA397988473

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8025218G>A (hg19) ; chr17:g.8121900G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121900G>A , CM000679.2:g.8121900G>A	GRCh38
NC_000017.10:g.8025218G>A , CM000679.1:g.8025218G>A	GRCh37
NC_000017.9:g.7965943G>A	NCBI36
NG_015807.1:g.2017C>T
NG_015816.1:g.7193C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.364C>T MANE Select	ENSP00000446205.2:p.Gln122Ter
ENST00000317814.8:c.349C>T	ENSP00000314774.4:p.Gln117Ter
ENST00000541682.6:c.364C>T	ENSP00000446205.2:p.Gln122Ter
ENST00000577735.1:c.340C>T	ENSP00000462491.1:p.Gln114Ter
NM_001165967.1:c.364C>T	NP_001159439.1:p.Gln122Ter
NM_032580.3:c.349C>T	NP_115969.2:p.Gln117Ter
XM_011524038.1:c.469C>T	XP_011522340.1:p.Gln157Ter
XM_011524039.1:c.460C>T	XP_011522341.1:p.Gln154Ter
XM_011524040.1:c.460C>T	XP_011522342.1:p.Gln154Ter
XM_011524041.1:c.451C>T	XP_011522343.1:p.Gln151Ter
XM_011524042.1:c.322C>T	XP_011522344.1:p.Gln108Ter
XR_934203.1:n.69+2086G>A
XM_017025232.1:c.469C>T	XP_016880721.1:p.Gln157Ter
XM_024451007.1:c.469C>T	XP_024306775.1:p.Gln157Ter
NM_001165967.2:c.364C>T MANE Select	NP_001159439.1:p.Gln122Ter
NM_032580.4:c.349C>T	NP_115969.2:p.Gln117Ter