Canonical Allele Identifier: CA2519056411
Gene: CHST3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008180_72008181insTG , CM000672.2:g.72008180_72008181insTG GRCh38
NC_000010.10:g.73767938_73767939insTG , CM000672.1:g.73767938_73767939insTG GRCh37
NC_000010.9:g.73437944_73437945insTG NCBI36
NG_012635.1:g.48819_48820insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1149_1150insTG MANE Select ENSP00000362207.4:p.Glu384TrpfsTer11
ENST00000373115.4:c.1149_1150insTG ENSP00000362207.4:p.Glu384TrpfsTer11
NM_004273.4:c.1149_1150insTG NP_004264.2:p.Glu384TrpfsTer11
XM_006718075.2:c.1149_1150insTG XP_006718138.1:p.Glu384TrpfsTer11
XM_011540369.1:c.1149_1150insTG XP_011538671.1:p.Glu384TrpfsTer11
XM_006718075.4:c.1149_1150insTG XP_006718138.1:p.Glu384TrpfsTer11
XM_011540369.2:c.1149_1150insTG XP_011538671.1:p.Glu384TrpfsTer11
NM_004273.5:c.1149_1150insTG MANE Select NP_004264.2:p.Glu384TrpfsTer11
Search 100 bp 5'
Search 100 bp 3'