Canonical Allele Identifier: CA397986941
Gene: HES7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8121596G>C , CM000679.2:g.8121596G>C GRCh38
NC_000017.10:g.8024914G>C , CM000679.1:g.8024914G>C GRCh37
NC_000017.9:g.7965639G>C NCBI36
NG_015807.1:g.2321C>G
NG_015816.1:g.7497C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000541682.7:c.668C>G MANE Select ENSP00000446205.2:p.Pro223Arg
ENST00000317814.8:c.653C>G ENSP00000314774.4:p.Pro218Arg
ENST00000541682.6:c.668C>G ENSP00000446205.2:p.Pro223Arg
NM_001165967.1:c.668C>G NP_001159439.1:p.Pro223Arg
NM_032580.3:c.653C>G NP_115969.2:p.Pro218Arg
XM_011524038.1:c.773C>G XP_011522340.1:p.Pro258Arg
XM_011524039.1:c.764C>G XP_011522341.1:p.Pro255Arg
XM_011524040.1:c.764C>G XP_011522342.1:p.Pro255Arg
XM_011524041.1:c.755C>G XP_011522343.1:p.Pro252Arg
XM_011524042.1:c.626C>G XP_011522344.1:p.Pro209Arg
XR_934203.1:n.69+1782G>C
XM_017025232.1:c.773C>G XP_016880721.1:p.Pro258Arg
XM_024451007.1:c.773C>G XP_024306775.1:p.Pro258Arg
NM_001165967.2:c.668C>G MANE Select NP_001159439.1:p.Pro223Arg
NM_032580.4:c.653C>G NP_115969.2:p.Pro218Arg