Canonical Allele Identifier: CA1918976845
Gene: CHST3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008290_72008293delinsACTC , CM000672.2:g.72008290_72008293delinsACTC GRCh38
NC_000010.10:g.73768048_73768051delinsACTC , CM000672.1:g.73768048_73768051delinsACTC GRCh37
NC_000010.9:g.73438054_73438057delinsACTC NCBI36
NG_012635.1:g.48929_48932delinsACTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1259_1262delinsACTC MANE Select ENSP00000362207.4:p.Asn420=
ENST00000373115.4:c.1259_1262delinsACTC ENSP00000362207.4:p.Asn420=
NM_004273.4:c.1259_1262delinsACTC NP_004264.2:p.Asn420=
XM_006718075.2:c.1259_1262delinsACTC XP_006718138.1:p.Asn420=
XM_011540369.1:c.1259_1262delinsACTC XP_011538671.1:p.Asn420=
XM_006718075.4:c.1259_1262delinsACTC XP_006718138.1:p.Asn420=
XM_011540369.2:c.1259_1262delinsACTC XP_011538671.1:p.Asn420=
NM_004273.5:c.1259_1262delinsACTC MANE Select NP_004264.2:p.Asn420=
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