Canonical Allele Identifier: CA2083133487
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33053925G= , CM000675.2:g.33053925G= GRCh38
NC_000013.10:g.33628062G= , CM000675.1:g.33628062G= GRCh37
NC_000013.9:g.32526062G= NCBI36
NG_011485.1:g.42492G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.978G= MANE Select ENSP00000369442.3:p.Trp326=
ENST00000380099.3:c.978G= ENSP00000369442.3:p.Trp326=
ENST00000487852.1:n.986G=
NM_004795.3:c.978G= NP_004786.2:p.Trp326=
XM_006719895.1:c.57G= XP_006719958.1:p.Trp19=
XM_006719895.2:c.57G= XP_006719958.1:p.Trp19=
NM_004795.4:c.978G= MANE Select NP_004786.2:p.Trp326=