Canonical Allele Identifier: CA929816958
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs1840090022

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009776_72009784del , CM000672.2:g.72009776_72009784del GRCh38
NC_000010.10:g.73769534_73769542del , CM000672.1:g.73769534_73769542del GRCh37
NC_000010.9:g.73439540_73439548del NCBI36
NG_012635.1:g.50415_50423del

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.*1305_*1313del MANE Select ENSP00000362207.4:n.*1305_*1313del
ENST00000373115.4:c.*1305_*1313del ENSP00000362207.4:n.*1305_*1313del
NM_004273.4:c.*1305_*1313del NP_004264.2:n.*1305_*1313del
XM_006718075.2:c.*1305_*1313del XP_006718138.1:n.*1305_*1313del
XM_011540369.1:c.*1305_*1313del XP_011538671.1:n.*1305_*1313del
XM_006718075.4:c.*1305_*1313del XP_006718138.1:n.*1305_*1313del
XM_011540369.2:c.*1305_*1313del XP_011538671.1:n.*1305_*1313del
NM_004273.5:c.*1305_*1313del MANE Select NP_004264.2:n.*1305_*1313del