Canonical Allele Identifier: CA1918975981
Gene: CHST3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007618_72007619delinsTC , CM000672.2:g.72007618_72007619delinsTC GRCh38
NC_000010.10:g.73767376_73767377delinsTC , CM000672.1:g.73767376_73767377delinsTC GRCh37
NC_000010.9:g.73437382_73437383delinsTC NCBI36
NG_012635.1:g.48257_48258delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.587_588delinsTC MANE Select ENSP00000362207.4:p.Phe196=
ENST00000373115.4:c.587_588delinsTC ENSP00000362207.4:p.Phe196=
NM_004273.4:c.587_588delinsTC NP_004264.2:p.Phe196=
XM_006718075.2:c.587_588delinsTC XP_006718138.1:p.Phe196=
XM_011540369.1:c.587_588delinsTC XP_011538671.1:p.Phe196=
XM_006718075.4:c.587_588delinsTC XP_006718138.1:p.Phe196=
XM_011540369.2:c.587_588delinsTC XP_011538671.1:p.Phe196=
NM_004273.5:c.587_588delinsTC MANE Select NP_004264.2:p.Phe196=
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