Canonical Allele Identifier: CA2541830907
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007785_72007829del , CM000672.2:g.72007785_72007829del GRCh38
NC_000010.10:g.73767543_73767587del , CM000672.1:g.73767543_73767587del GRCh37
NC_000010.9:g.73437549_73437593del NCBI36
NG_012635.1:g.48424_48468del

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.754_798del MANE Select ENSP00000362207.4:p.Cys252_Arg266del
ENST00000373115.4:c.754_798del ENSP00000362207.4:p.Cys252_Arg266del
NM_004273.4:c.754_798del NP_004264.2:p.Cys252_Arg266del
XM_006718075.2:c.754_798del XP_006718138.1:p.Cys252_Arg266del
XM_011540369.1:c.754_798del XP_011538671.1:p.Cys252_Arg266del
XM_006718075.4:c.754_798del XP_006718138.1:p.Cys252_Arg266del
XM_011540369.2:c.754_798del XP_011538671.1:p.Cys252_Arg266del
NM_004273.5:c.754_798del MANE Select NP_004264.2:p.Cys252_Arg266del