Canonical Allele Identifier: CA2083142840
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036116C= , CM000675.2:g.33036116C= GRCh38
NC_000013.10:g.33610253C= , CM000675.1:g.33610253C= GRCh37
NC_000013.9:g.32508253C= NCBI36
NG_011485.1:g.24683C=

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17651C= MANE Select ENSP00000369442.3:n.820-17651C=
ENST00000380099.3:c.820-17651C= ENSP00000369442.3:n.820-17651C=
ENST00000487852.1:n.828-17651C=
NM_004795.3:c.820-17651C= NP_004786.2:n.820-17651C=
XM_006719895.1:c.-102-17651C= XP_006719958.1:n.-102-17651C=
XM_006719895.2:c.-102-17651C= XP_006719958.1:n.-102-17651C=
NM_004795.4:c.820-17651C= MANE Select NP_004786.2:n.820-17651C=