Canonical Allele Identifier: CA1918976798
Gene: CHST3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008208_72008209delinsCT , CM000672.2:g.72008208_72008209delinsCT GRCh38
NC_000010.10:g.73767966_73767967delinsCT , CM000672.1:g.73767966_73767967delinsCT GRCh37
NC_000010.9:g.73437972_73437973delinsCT NCBI36
NG_012635.1:g.48847_48848delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1177_1178delinsCT MANE Select ENSP00000362207.4:p.Leu393=
ENST00000373115.4:c.1177_1178delinsCT ENSP00000362207.4:p.Leu393=
NM_004273.4:c.1177_1178delinsCT NP_004264.2:p.Leu393=
XM_006718075.2:c.1177_1178delinsCT XP_006718138.1:p.Leu393=
XM_011540369.1:c.1177_1178delinsCT XP_011538671.1:p.Leu393=
XM_006718075.4:c.1177_1178delinsCT XP_006718138.1:p.Leu393=
XM_011540369.2:c.1177_1178delinsCT XP_011538671.1:p.Leu393=
NM_004273.5:c.1177_1178delinsCT MANE Select NP_004264.2:p.Leu393=
Search 100 bp 5'
Search 100 bp 3'