Canonical Allele Identifier: CA2635936709
Gene: HES7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8121612_8121623del , CM000679.2:g.8121612_8121623del GRCh38
NC_000017.10:g.8024930_8024941del , CM000679.1:g.8024930_8024941del GRCh37
NC_000017.9:g.7965655_7965666del NCBI36
NG_015807.1:g.2297_2308del
NG_015816.1:g.7473_7484del

Transcript Alleles

HGVS Amino-acid Change
ENST00000541682.7:c.644_655del MANE Select ENSP00000446205.2:p.Pro215_Pro218del
ENST00000317814.8:c.629_640del ENSP00000314774.4:p.Pro210_Pro213del
ENST00000541682.6:c.644_655del ENSP00000446205.2:p.Pro215_Pro218del
NM_001165967.1:c.644_655del NP_001159439.1:p.Pro215_Pro218del
NM_032580.3:c.629_640del NP_115969.2:p.Pro210_Pro213del
XM_011524038.1:c.749_760del XP_011522340.1:p.Pro250_Pro253del
XM_011524039.1:c.740_751del XP_011522341.1:p.Pro247_Pro250del
XM_011524040.1:c.740_751del XP_011522342.1:p.Pro247_Pro250del
XM_011524041.1:c.731_742del XP_011522343.1:p.Pro244_Pro247del
XM_011524042.1:c.602_613del XP_011522344.1:p.Pro201_Pro204del
XR_934203.1:n.69+1798_69+1809del
XM_017025232.1:c.749_760del XP_016880721.1:p.Pro250_Pro253del
XM_024451007.1:c.749_760del XP_024306775.1:p.Pro250_Pro253del
NM_001165967.2:c.644_655del MANE Select NP_001159439.1:p.Pro215_Pro218del
NM_032580.4:c.629_640del NP_115969.2:p.Pro210_Pro213del