Canonical Allele Identifier: CA1918976823
Gene: CHST3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008260_72008266delinsACGGCAG , CM000672.2:g.72008260_72008266delinsACGGCAG GRCh38
NC_000010.10:g.73768018_73768024delinsACGGCAG , CM000672.1:g.73768018_73768024delinsACGGCAG GRCh37
NC_000010.9:g.73438024_73438030delinsACGGCAG NCBI36
NG_012635.1:g.48899_48905delinsACGGCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1229_1235delinsACGGCAG MANE Select ENSP00000362207.4:p.Asp410=
ENST00000373115.4:c.1229_1235delinsACGGCAG ENSP00000362207.4:p.Asp410=
NM_004273.4:c.1229_1235delinsACGGCAG NP_004264.2:p.Asp410=
XM_006718075.2:c.1229_1235delinsACGGCAG XP_006718138.1:p.Asp410=
XM_011540369.1:c.1229_1235delinsACGGCAG XP_011538671.1:p.Asp410=
XM_006718075.4:c.1229_1235delinsACGGCAG XP_006718138.1:p.Asp410=
XM_011540369.2:c.1229_1235delinsACGGCAG XP_011538671.1:p.Asp410=
NM_004273.5:c.1229_1235delinsACGGCAG MANE Select NP_004264.2:p.Asp410=
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