Canonical Allele Identifier: CA1140384176
Gene: CHI3L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203182297G= , CM000663.2:g.203182297G= GRCh38
NC_000001.10:g.203151425G= , CM000663.1:g.203151425G= GRCh37
NC_000001.9:g.201418048G= NCBI36
NG_013056.1:g.9498C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000255409.8:c.587+434C= MANE Select ENSP00000255409.3:n.587+434C=
ENST00000255409.7:c.587+434C= ENSP00000255409.3:n.587+434C=
ENST00000404436.2:c.75+434C=
ENST00000472064.1:n.111+434C=
NM_001276.2:c.587+434C= NP_001267.2:n.587+434C=
XM_011509105.1:c.605+434C= XP_011507407.1:n.605+434C=
XM_011509106.1:c.605+434C= XP_011507408.1:n.605+434C=
XM_011509107.1:c.587+434C= XP_011507409.1:n.587+434C=
XM_011509108.1:c.605+434C= XP_011507410.1:n.605+434C=
NM_001276.3:c.587+434C= NP_001267.2:n.587+434C=
NM_001276.4:c.587+434C= MANE Select NP_001267.2:n.587+434C=