Canonical Allele Identifier: CA2609582001
Gene: CHST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007803_72007883dup , CM000672.2:g.72007803_72007883dup GRCh38
NC_000010.10:g.73767561_73767641dup , CM000672.1:g.73767561_73767641dup GRCh37
NC_000010.9:g.73437567_73437647dup NCBI36
NG_012635.1:g.48442_48522dup

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.772_852dup MANE Select ENSP00000362207.4:p.Gln284_Pro285insThrLe...
ENST00000373115.4:c.772_852dup ENSP00000362207.4:p.Gln284_Pro285insThrLe...
NM_004273.4:c.772_852dup NP_004264.2:p.Gln284_Pro285insThrLeuAlaAl...
XM_006718075.2:c.772_852dup XP_006718138.1:p.Gln284_Pro285insThrLeuAl...
XM_011540369.1:c.772_852dup XP_011538671.1:p.Gln284_Pro285insThrLeuAl...
XM_006718075.4:c.772_852dup XP_006718138.1:p.Gln284_Pro285insThrLeuAl...
XM_011540369.2:c.772_852dup XP_011538671.1:p.Gln284_Pro285insThrLeuAl...
NM_004273.5:c.772_852dup MANE Select NP_004264.2:p.Gln284_Pro285insThrLeuAlaAl...