Canonical Allele Identifier: CA397988505
Gene: HES7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8121909C>G , CM000679.2:g.8121909C>G GRCh38
NC_000017.10:g.8025227C>G , CM000679.1:g.8025227C>G GRCh37
NC_000017.9:g.7965952C>G NCBI36
NG_015807.1:g.2008G>C
NG_015816.1:g.7184G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000541682.7:c.355G>C MANE Select ENSP00000446205.2:p.Ala119Pro
ENST00000317814.8:c.340G>C ENSP00000314774.4:p.Ala114Pro
ENST00000541682.6:c.355G>C ENSP00000446205.2:p.Ala119Pro
ENST00000577735.1:c.331G>C ENSP00000462491.1:p.Ala111Pro
NM_001165967.1:c.355G>C NP_001159439.1:p.Ala119Pro
NM_032580.3:c.340G>C NP_115969.2:p.Ala114Pro
XM_011524038.1:c.460G>C XP_011522340.1:p.Ala154Pro
XM_011524039.1:c.451G>C XP_011522341.1:p.Ala151Pro
XM_011524040.1:c.451G>C XP_011522342.1:p.Ala151Pro
XM_011524041.1:c.442G>C XP_011522343.1:p.Ala148Pro
XM_011524042.1:c.313G>C XP_011522344.1:p.Ala105Pro
XR_934203.1:n.69+2095C>G
XM_017025232.1:c.460G>C XP_016880721.1:p.Ala154Pro
XM_024451007.1:c.460G>C XP_024306775.1:p.Ala154Pro
NM_001165967.2:c.355G>C MANE Select NP_001159439.1:p.Ala119Pro
NM_032580.4:c.340G>C NP_115969.2:p.Ala114Pro