Canonical Allele Identifier: CA2574581749
Gene: CHST3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007651_72007653del , CM000672.2:g.72007651_72007653del GRCh38
NC_000010.10:g.73767409_73767411del , CM000672.1:g.73767409_73767411del GRCh37
NC_000010.9:g.73437415_73437417del NCBI36
NG_012635.1:g.48290_48292del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.620_622del MANE Select ENSP00000362207.4:p.Ile207del
ENST00000373115.4:c.620_622del ENSP00000362207.4:p.Ile207del
NM_004273.4:c.620_622del NP_004264.2:p.Ile207del
XM_006718075.2:c.620_622del XP_006718138.1:p.Ile207del
XM_011540369.1:c.620_622del XP_011538671.1:p.Ile207del
XM_006718075.4:c.620_622del XP_006718138.1:p.Ile207del
XM_011540369.2:c.620_622del XP_011538671.1:p.Ile207del
NM_004273.5:c.620_622del MANE Select NP_004264.2:p.Ile207del
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