Canonical Allele Identifier: CA397990891

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8123083T>C , CM000679.2:g.8123083T>C	GRCh38
NC_000017.10:g.8026401T>C , CM000679.1:g.8026401T>C	GRCh37
NC_000017.9:g.7967126T>C	NCBI36
NG_015807.1:g.834A>G
NG_015816.1:g.6010A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001165967.2:c.86A>G MANE Select	NP_001159439.1:p.Asn29Ser
ENST00000541682.7:c.86A>G MANE Select	ENSP00000446205.2:p.Asn29Ser
NM_001165967.1:c.86A>G	NP_001159439.1:p.Asn29Ser
NM_032580.3:c.86A>G	NP_115969.2:p.Asn29Ser
NM_032580.4:c.86A>G	NP_115969.2:p.Asn29Ser
ENST00000317814.8:c.86A>G	ENSP00000314774.4:p.Asn29Ser
ENST00000541682.6:c.86A>G	ENSP00000446205.2:p.Asn29Ser
ENST00000577735.1:c.62A>G	ENSP00000462491.1:p.Asn21Ser
XM_011524038.1:c.191A>G	XP_011522340.1:p.Asn64Ser
XM_011524039.1:c.182A>G	XP_011522341.1:p.Asn61Ser
XM_011524040.1:c.182A>G	XP_011522342.1:p.Asn61Ser
XM_011524041.1:c.173A>G	XP_011522343.1:p.Asn58Ser
XM_011524042.1:c.44A>G	XP_011522344.1:p.Asn15Ser
XM_017025232.1:c.191A>G	XP_016880721.1:p.Asn64Ser
XM_024451007.1:c.191A>G	XP_024306775.1:p.Asn64Ser
XR_934203.1:n.69+3269T>C