Canonical Allele Identifier: CA2695212416
Gene: CHST3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007648_72007649delinsGA , CM000672.2:g.72007648_72007649delinsGA GRCh38
NC_000010.10:g.73767406_73767407delinsGA , CM000672.1:g.73767406_73767407delinsGA GRCh37
NC_000010.9:g.73437412_73437413delinsGA NCBI36
NG_012635.1:g.48287_48288delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.617_618delinsGA MANE Select ENSP00000362207.4:p.Phe206Ter
ENST00000373115.4:c.617_618delinsGA ENSP00000362207.4:p.Phe206Ter
NM_004273.4:c.617_618delinsGA NP_004264.2:p.Phe206Ter
XM_006718075.2:c.617_618delinsGA XP_006718138.1:p.Phe206Ter
XM_011540369.1:c.617_618delinsGA XP_011538671.1:p.Phe206Ter
XM_006718075.4:c.617_618delinsGA XP_006718138.1:p.Phe206Ter
XM_011540369.2:c.617_618delinsGA XP_011538671.1:p.Phe206Ter
NM_004273.5:c.617_618delinsGA MANE Select NP_004264.2:p.Phe206Ter
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