Canonical Allele Identifier: CA1146245484
Gene: CHI3L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203183505G= , CM000663.2:g.203183505G= GRCh38
NC_000001.10:g.203152633G= , CM000663.1:g.203152633G= GRCh37
NC_000001.9:g.201419256G= NCBI36
NG_013056.1:g.8290C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000255409.8:c.465+136C= MANE Select ENSP00000255409.3:n.465+136C=
ENST00000255409.7:c.465+136C= ENSP00000255409.3:n.465+136C=
NM_001276.2:c.465+136C= NP_001267.2:n.465+136C=
XM_011509105.1:c.483+136C= XP_011507407.1:n.483+136C=
XM_011509106.1:c.483+136C= XP_011507408.1:n.483+136C=
XM_011509107.1:c.465+136C= XP_011507409.1:n.465+136C=
XM_011509108.1:c.483+136C= XP_011507410.1:n.483+136C=
NM_001276.3:c.465+136C= NP_001267.2:n.465+136C=
NM_001276.4:c.465+136C= MANE Select NP_001267.2:n.465+136C=