Canonical Allele Identifier: CA645561183
Gene: CHST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007812dup , CM000672.2:g.72007812dup GRCh38
NC_000010.10:g.73767570dup , CM000672.1:g.73767570dup GRCh37
NC_000010.9:g.73437576dup NCBI36
NG_012635.1:g.48451dup

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.781dup MANE Select ENSP00000362207.4:p.Ala261GlyfsTer?
ENST00000373115.4:c.781dup ENSP00000362207.4:p.Ala261GlyfsTer?
NM_004273.4:c.781dup NP_004264.2:p.Ala261GlyfsTer?
XM_006718075.2:c.781dup XP_006718138.1:p.Ala261GlyfsTer?
XM_011540369.1:c.781dup XP_011538671.1:p.Ala261GlyfsTer?
XM_006718075.4:c.781dup XP_006718138.1:p.Ala261GlyfsTer?
XM_011540369.2:c.781dup XP_011538671.1:p.Ala261GlyfsTer?
NM_004273.5:c.781dup MANE Select NP_004264.2:p.Ala261GlyfsTer?