Canonical Allele Identifier: CA2083142821
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036093G= , CM000675.2:g.33036093G= GRCh38
NC_000013.10:g.33610230G= , CM000675.1:g.33610230G= GRCh37
NC_000013.9:g.32508230G= NCBI36
NG_011485.1:g.24660G=

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17674G= MANE Select ENSP00000369442.3:n.820-17674G=
ENST00000380099.3:c.820-17674G= ENSP00000369442.3:n.820-17674G=
ENST00000487852.1:n.828-17674G=
NM_004795.3:c.820-17674G= NP_004786.2:n.820-17674G=
XM_006719895.1:c.-102-17674G= XP_006719958.1:n.-102-17674G=
XM_006719895.2:c.-102-17674G= XP_006719958.1:n.-102-17674G=
NM_004795.4:c.820-17674G= MANE Select NP_004786.2:n.820-17674G=