Canonical Allele Identifier: CA2788492310
Gene: CHST3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007663_72007666del , CM000672.2:g.72007663_72007666del GRCh38
NC_000010.10:g.73767421_73767424del , CM000672.1:g.73767421_73767424del GRCh37
NC_000010.9:g.73437427_73437430del NCBI36
NG_012635.1:g.48302_48305del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.632_635del MANE Select ENSP00000362207.4:p.Pro211ArgfsTer4
ENST00000373115.4:c.632_635del ENSP00000362207.4:p.Pro211ArgfsTer4
NM_004273.4:c.632_635del NP_004264.2:p.Pro211ArgfsTer4
XM_006718075.2:c.632_635del XP_006718138.1:p.Pro211ArgfsTer4
XM_011540369.1:c.632_635del XP_011538671.1:p.Pro211ArgfsTer4
XM_006718075.4:c.632_635del XP_006718138.1:p.Pro211ArgfsTer4
XM_011540369.2:c.632_635del XP_011538671.1:p.Pro211ArgfsTer4
NM_004273.5:c.632_635del MANE Select NP_004264.2:p.Pro211ArgfsTer4
Search 100 bp 5'
Search 100 bp 3'