Canonical Allele Identifier: CA730274480
Gene: CHI3L1 HGNC NCBI

Linked Data

dbSNP Id: rs1300632880

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203183673del , CM000663.2:g.203183673del GRCh38
NC_000001.10:g.203152801del , CM000663.1:g.203152801del GRCh37
NC_000001.9:g.201419424del NCBI36
NG_013056.1:g.8122del

Transcript Alleles

HGVS Amino-acid change
ENST00000255409.8:c.433del MANE Select ENSP00000255409.3:p.Arg145GlufsTer9
ENST00000255409.7:c.433del ENSP00000255409.3:p.Arg145GlufsTer9
NM_001276.2:c.433del NP_001267.2:p.Arg145GlufsTer9
XM_011509105.1:c.451del XP_011507407.1:p.Arg151GlufsTer9
XM_011509106.1:c.451del XP_011507408.1:p.Arg151GlufsTer9
XM_011509107.1:c.433del XP_011507409.1:p.Arg145GlufsTer9
XM_011509108.1:c.451del XP_011507410.1:p.Arg151GlufsTer9
NM_001276.3:c.433del NP_001267.2:p.Arg145GlufsTer9
NM_001276.4:c.433del MANE Select NP_001267.2:p.Arg145GlufsTer9