Canonical Allele Identifier: CA397987336
Gene: HES7 HGNC NCBI

Linked Data

gnomAD v4: 17-8121675-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8121675G>T , CM000679.2:g.8121675G>T GRCh38
NC_000017.10:g.8024993G>T , CM000679.1:g.8024993G>T GRCh37
NC_000017.9:g.7965718G>T NCBI36
NG_015807.1:g.2242C>A
NG_015816.1:g.7418C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000541682.7:c.589C>A MANE Select ENSP00000446205.2:p.Pro197Thr
ENST00000317814.8:c.574C>A ENSP00000314774.4:p.Pro192Thr
ENST00000541682.6:c.589C>A ENSP00000446205.2:p.Pro197Thr
NM_001165967.1:c.589C>A NP_001159439.1:p.Pro197Thr
NM_032580.3:c.574C>A NP_115969.2:p.Pro192Thr
XM_011524038.1:c.694C>A XP_011522340.1:p.Pro232Thr
XM_011524039.1:c.685C>A XP_011522341.1:p.Pro229Thr
XM_011524040.1:c.685C>A XP_011522342.1:p.Pro229Thr
XM_011524041.1:c.676C>A XP_011522343.1:p.Pro226Thr
XM_011524042.1:c.547C>A XP_011522344.1:p.Pro183Thr
XR_934203.1:n.69+1861G>T
XM_017025232.1:c.694C>A XP_016880721.1:p.Pro232Thr
XM_024451007.1:c.694C>A XP_024306775.1:p.Pro232Thr
NM_001165967.2:c.589C>A MANE Select NP_001159439.1:p.Pro197Thr
NM_032580.4:c.574C>A NP_115969.2:p.Pro192Thr