Canonical Allele Identifier: CA2609583234
Gene: CHST3 HGNC NCBI

Linked Data

gnomAD v4: 10-72008150-C-CGTGGCACGCGGGCCGCTGCAG
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008151_72008171dup , CM000672.2:g.72008151_72008171dup GRCh38
NC_000010.10:g.73767909_73767929dup , CM000672.1:g.73767909_73767929dup GRCh37
NC_000010.9:g.73437915_73437935dup NCBI36
NG_012635.1:g.48790_48810dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1120_1140dup MANE Select ENSP00000362207.4:p.Gln380_Lys381insValAlaArgGlyProLeuGln
ENST00000373115.4:c.1120_1140dup ENSP00000362207.4:p.Gln380_Lys381insValAlaArgGlyProLeuGln
NM_004273.4:c.1120_1140dup NP_004264.2:p.Gln380_Lys381insValAlaArgGlyProLeuGln
XM_006718075.2:c.1120_1140dup XP_006718138.1:p.Gln380_Lys381insValAlaArgGlyProLeuGln
XM_011540369.1:c.1120_1140dup XP_011538671.1:p.Gln380_Lys381insValAlaArgGlyProLeuGln
XM_006718075.4:c.1120_1140dup XP_006718138.1:p.Gln380_Lys381insValAlaArgGlyProLeuGln
XM_011540369.2:c.1120_1140dup XP_011538671.1:p.Gln380_Lys381insValAlaArgGlyProLeuGln
NM_004273.5:c.1120_1140dup MANE Select NP_004264.2:p.Gln380_Lys381insValAlaArgGlyProLeuGln
Search 100 bp 5'
Search 100 bp 3'