Canonical Allele Identifier: CA2788492307
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007659_72007660del , CM000672.2:g.72007659_72007660del GRCh38
NC_000010.10:g.73767417_73767418del , CM000672.1:g.73767417_73767418del GRCh37
NC_000010.9:g.73437423_73437424del NCBI36
NG_012635.1:g.48298_48299del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.628_629del MANE Select ENSP00000362207.4:p.Leu210AlafsTer?
ENST00000373115.4:c.628_629del ENSP00000362207.4:p.Leu210AlafsTer?
NM_004273.4:c.628_629del NP_004264.2:p.Leu210AlafsTer?
XM_006718075.2:c.628_629del XP_006718138.1:p.Leu210AlafsTer?
XM_011540369.1:c.628_629del XP_011538671.1:p.Leu210AlafsTer?
XM_006718075.4:c.628_629del XP_006718138.1:p.Leu210AlafsTer?
XM_011540369.2:c.628_629del XP_011538671.1:p.Leu210AlafsTer?
NM_004273.5:c.628_629del MANE Select NP_004264.2:p.Leu210AlafsTer?