Canonical Allele Identifier: CA397988570

Gene: HES7

Linked Data

• gnomAD v4: 17-8121924-C-A
• MyVariant Identifiers: chr17:g.8025242C>A (hg19) ; chr17:g.8121924C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121924C>A , CM000679.2:g.8121924C>A	GRCh38
NC_000017.10:g.8025242C>A , CM000679.1:g.8025242C>A	GRCh37
NC_000017.9:g.7965967C>A	NCBI36
NG_015807.1:g.1993G>T
NG_015816.1:g.7169G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.340G>T MANE Select	ENSP00000446205.2:p.Asp114Tyr
ENST00000317814.8:c.325G>T	ENSP00000314774.4:p.Asp109Tyr
ENST00000541682.6:c.340G>T	ENSP00000446205.2:p.Asp114Tyr
ENST00000577735.1:c.316G>T	ENSP00000462491.1:p.Asp106Tyr
NM_001165967.1:c.340G>T	NP_001159439.1:p.Asp114Tyr
NM_032580.3:c.325G>T	NP_115969.2:p.Asp109Tyr
XM_011524038.1:c.445G>T	XP_011522340.1:p.Asp149Tyr
XM_011524039.1:c.436G>T	XP_011522341.1:p.Asp146Tyr
XM_011524040.1:c.436G>T	XP_011522342.1:p.Asp146Tyr
XM_011524041.1:c.427G>T	XP_011522343.1:p.Asp143Tyr
XM_011524042.1:c.298G>T	XP_011522344.1:p.Asp100Tyr
XR_934203.1:n.69+2110C>A
XM_017025232.1:c.445G>T	XP_016880721.1:p.Asp149Tyr
XM_024451007.1:c.445G>T	XP_024306775.1:p.Asp149Tyr
NM_001165967.2:c.340G>T MANE Select	NP_001159439.1:p.Asp114Tyr
NM_032580.4:c.325G>T	NP_115969.2:p.Asp109Tyr