Canonical Allele Identifier: CA2788492385
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008240_72008241insCGCC , CM000672.2:g.72008240_72008241insCGCC GRCh38
NC_000010.10:g.73767998_73767999insCGCC , CM000672.1:g.73767998_73767999insCGCC GRCh37
NC_000010.9:g.73438004_73438005insCGCC NCBI36
NG_012635.1:g.48879_48880insCGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1209_1210insCGCC MANE Select ENSP00000362207.4:p.Asn404ArgfsTer?
ENST00000373115.4:c.1209_1210insCGCC ENSP00000362207.4:p.Asn404ArgfsTer?
NM_004273.4:c.1209_1210insCGCC NP_004264.2:p.Asn404ArgfsTer?
XM_006718075.2:c.1209_1210insCGCC XP_006718138.1:p.Asn404ArgfsTer?
XM_011540369.1:c.1209_1210insCGCC XP_011538671.1:p.Asn404ArgfsTer?
XM_006718075.4:c.1209_1210insCGCC XP_006718138.1:p.Asn404ArgfsTer?
XM_011540369.2:c.1209_1210insCGCC XP_011538671.1:p.Asn404ArgfsTer?
NM_004273.5:c.1209_1210insCGCC MANE Select NP_004264.2:p.Asn404ArgfsTer?