Canonical Allele Identifier: CA1918976525
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007914_72007924delinsCGCGTCATCCA , CM000672.2:g.72007914_72007924delinsCGCGTCATCCA GRCh38
NC_000010.10:g.73767672_73767682delinsCGCGTCATCCA , CM000672.1:g.73767672_73767682delinsCGCGTCATCCA GRCh37
NC_000010.9:g.73437678_73437688delinsCGCGTCATCCA NCBI36
NG_012635.1:g.48553_48563delinsCGCGTCATCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.883_893delinsCGCGTCATCCA MANE Select ENSP00000362207.4:p.Arg295=
ENST00000373115.4:c.883_893delinsCGCGTCATCCA ENSP00000362207.4:p.Arg295=
NM_004273.4:c.883_893delinsCGCGTCATCCA NP_004264.2:p.Arg295=
XM_006718075.2:c.883_893delinsCGCGTCATCCA XP_006718138.1:p.Arg295=
XM_011540369.1:c.883_893delinsCGCGTCATCCA XP_011538671.1:p.Arg295=
XM_006718075.4:c.883_893delinsCGCGTCATCCA XP_006718138.1:p.Arg295=
XM_011540369.2:c.883_893delinsCGCGTCATCCA XP_011538671.1:p.Arg295=
NM_004273.5:c.883_893delinsCGCGTCATCCA MANE Select NP_004264.2:p.Arg295=