Canonical Allele Identifier: CA2788492415
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009226_72009231del , CM000672.2:g.72009226_72009231del GRCh38
NC_000010.10:g.73768984_73768989del , CM000672.1:g.73768984_73768989del GRCh37
NC_000010.9:g.73438990_73438995del NCBI36
NG_012635.1:g.49865_49870del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*755_*760del MANE Select ENSP00000362207.4:n.*755_*760del
ENST00000373115.4:c.*755_*760del ENSP00000362207.4:n.*755_*760del
NM_004273.4:c.*755_*760del NP_004264.2:n.*755_*760del
XM_006718075.2:c.*755_*760del XP_006718138.1:n.*755_*760del
XM_011540369.1:c.*755_*760del XP_011538671.1:n.*755_*760del
XM_006718075.4:c.*755_*760del XP_006718138.1:n.*755_*760del
XM_011540369.2:c.*755_*760del XP_011538671.1:n.*755_*760del
NM_004273.5:c.*755_*760del MANE Select NP_004264.2:n.*755_*760del