Canonical Allele Identifier: CA377151536
Gene: CHST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008208C>G , CM000672.2:g.72008208C>G GRCh38
NC_000010.10:g.73767966C>G , CM000672.1:g.73767966C>G GRCh37
NC_000010.9:g.73437972C>G NCBI36
NG_012635.1:g.48847C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1177C>G MANE Select ENSP00000362207.4:p.Leu393Val
ENST00000373115.4:c.1177C>G ENSP00000362207.4:p.Leu393Val
NM_004273.4:c.1177C>G NP_004264.2:p.Leu393Val
XM_006718075.2:c.1177C>G XP_006718138.1:p.Leu393Val
XM_011540369.1:c.1177C>G XP_011538671.1:p.Leu393Val
XM_006718075.4:c.1177C>G XP_006718138.1:p.Leu393Val
XM_011540369.2:c.1177C>G XP_011538671.1:p.Leu393Val
NM_004273.5:c.1177C>G MANE Select NP_004264.2:p.Leu393Val