Canonical Allele Identifier: CA645561182
Gene: CHST3 HGNC NCBI

Linked Data

gnomAD v4: 10-72007745-CAAG-C
COSMIC: COSM427862
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007749_72007751del , CM000672.2:g.72007749_72007751del GRCh38
NC_000010.10:g.73767507_73767509del , CM000672.1:g.73767507_73767509del GRCh37
NC_000010.9:g.73437513_73437515del NCBI36
NG_012635.1:g.48388_48390del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.718_720del MANE Select ENSP00000362207.4:p.Lys240del
ENST00000373115.4:c.718_720del ENSP00000362207.4:p.Lys240del
NM_004273.4:c.718_720del NP_004264.2:p.Lys240del
XM_006718075.2:c.718_720del XP_006718138.1:p.Lys240del
XM_011540369.1:c.718_720del XP_011538671.1:p.Lys240del
XM_006718075.4:c.718_720del XP_006718138.1:p.Lys240del
XM_011540369.2:c.718_720del XP_011538671.1:p.Lys240del
NM_004273.5:c.718_720del MANE Select NP_004264.2:p.Lys240del
Search 100 bp 5'
Search 100 bp 3'